Canonical Allele Identifier: CA467424164

Gene: POMT1

Linked Data

• gnomAD v4: 9-131522971-G-T
• MyVariant Identifiers: chr9:g.134398358G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.131522971G>T , CM000671.2:g.131522971G>T	GRCh38
NC_000009.11:g.134398358G>T , CM000671.1:g.134398358G>T	GRCh37
NC_000009.10:g.133388179G>T	NCBI36
NG_008896.1:g.25070G>T
NG_008896.2:g.25070G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341012.13:c.1881G>T	ENSP00000343034.7:p.Val627=
ENST00000404875.7:n.2583G>T
ENST00000423007.6:c.2100G>T	ENSP00000404119.2:p.Val700=
ENST00000677295.2:c.*2387G>T	ENSP00000504346.2:n.*2387G>T
ENST00000678264.2:c.*2226G>T	ENSP00000503157.2:n.*2226G>T
ENST00000682070.1:n.2353G>T
ENST00000682639.1:c.40G>T
ENST00000682813.1:n.2440G>T
ENST00000683231.1:c.40G>T
ENST00000683392.1:n.4635G>T
ENST00000683712.1:n.2448G>T
ENST00000683900.1:n.3943G>T
ENST00000684062.1:n.2709G>T
ENST00000684399.1:c.40G>T
ENST00000684579.1:n.3889G>T
ENST00000341012.12:c.1881G>T	ENSP00000343034.7:p.Val627=
ENST00000372220.5:c.912G>T	ENSP00000361294.5:p.Val304=
ENST00000372228.9:c.2109G>T	ENSP00000361302.3:p.Val703=
ENST00000402686.8:c.2043G>T MANE Select	ENSP00000385797.4:p.Val681=
ENST00000676640.1:c.2043G>T	ENSP00000503281.1:p.Val681=
ENST00000676803.1:c.1104G>T	ENSP00000503093.1:p.Val368=
ENST00000676835.1:c.*1258G>T	ENSP00000502911.1:n.*1258G>T
ENST00000677029.1:c.1587G>T	ENSP00000502936.1:p.Val529=
ENST00000677099.1:c.*1753G>T	ENSP00000504553.1:n.*1753G>T
ENST00000677216.1:c.1692G>T	ENSP00000503772.1:p.Val564=
ENST00000677221.1:n.1068G>T
ENST00000677295.1:c.*1265G>T	ENSP00000504346.1:n.*1265G>T
ENST00000677444.1:c.1988G>T
ENST00000677586.1:n.1410G>T
ENST00000677626.1:c.1692G>T	ENSP00000503552.1:p.Val564=
ENST00000677853.1:c.*1051G>T	ENSP00000503488.1:n.*1051G>T
ENST00000678264.1:c.*1420G>T	ENSP00000503157.1:n.*1420G>T
ENST00000678303.1:c.1953G>T	ENSP00000503696.1:p.Val651=
ENST00000678366.1:c.*2292G>T	ENSP00000504353.1:n.*2292G>T
ENST00000678546.1:c.*1988G>T	ENSP00000503062.1:n.*1988G>T
ENST00000678548.1:c.*2182G>T	ENSP00000503934.1:n.*2182G>T
ENST00000678626.1:n.1879G>T
ENST00000678739.1:c.*2209G>T	ENSP00000503806.1:n.*2209G>T
ENST00000678833.1:c.*1795G>T	ENSP00000503893.1:n.*1795G>T
ENST00000679023.1:c.1881G>T	ENSP00000503718.1:p.Val627=
ENST00000679076.1:c.1662G>T
ENST00000679111.1:c.*799G>T	ENSP00000504257.1:n.*799G>T
ENST00000679189.1:c.1692G>T	ENSP00000503356.1:p.Val564=
ENST00000341012.11:c.1881G>T	ENSP00000343034.7:p.Val627=
ENST00000372220.4:c.906G>T	ENSP00000361294.4:p.Val302=
ENST00000372228.7:c.2109G>T	ENSP00000361302.3:p.Val703=
ENST00000402686.7:c.2043G>T	ENSP00000385797.3:p.Val681=
ENST00000404875.6:c.1692G>T	ENSP00000384531.2:p.Val564=
ENST00000423007.5:c.2043G>T	ENSP00000404119.1:p.Val681=
ENST00000485278.5:n.2593G>T
NM_001077365.1:c.2043G>T	NP_001070833.1:p.Val681=
NM_001077366.1:c.1881G>T	NP_001070834.1:p.Val627=
NM_001136113.1:c.2043G>T	NP_001129585.1:p.Val681=
NM_001136114.1:c.1692G>T	NP_001129586.1:p.Val564=
NM_007171.3:c.2109G>T	NP_009102.3:p.Val703=
XM_005272156.1:c.2109G>T	XP_005272213.1:p.Val703=
XM_005272158.1:c.1947G>T	XP_005272215.1:p.Val649=
XM_005272159.1:c.1758G>T	XP_005272216.1:p.Val586=
XM_005272162.1:c.912G>T	XP_005272219.1:p.Val304=
XM_006716932.1:c.1758G>T	XP_006716995.1:p.Val586=
XM_011518140.1:c.1962G>T	XP_011516442.1:p.Val654=
XM_011518141.1:c.1896G>T	XP_011516443.1:p.Val632=
XM_011518142.1:c.1800G>T	XP_011516444.1:p.Val600=
XM_011518143.1:c.1794G>T	XP_011516445.1:p.Val598=
XM_011518145.1:c.1653G>T	XP_011516447.1:p.Val551=
XM_011518147.1:c.981G>T	XP_011516449.1:p.Val327=
XR_929703.1:n.2285G>T
NM_001353193.1:c.2109G>T	NP_001340122.1:p.Val703=
NM_001353194.1:c.1881G>T	NP_001340123.1:p.Val627=
NM_001353195.1:c.1692G>T	NP_001340124.1:p.Val564=
NM_001353196.1:c.1953G>T	NP_001340125.1:p.Val651=
NM_001353197.1:c.1947G>T	NP_001340126.1:p.Val649=
NM_001353198.1:c.1947G>T	NP_001340127.1:p.Val649=
NM_001353199.1:c.1758G>T	NP_001340128.1:p.Val586=
NM_001353200.1:c.1587G>T	NP_001340129.1:p.Val529=
NR_148391.1:n.2093G>T
NR_148392.1:n.2311G>T
NR_148393.1:n.2232G>T
NR_148394.1:n.1986G>T
NR_148395.1:n.2384G>T
NR_148396.1:n.2018G>T
NR_148397.1:n.2143G>T
NR_148398.1:n.2098G>T
NR_148399.1:n.2624G>T
NR_148400.1:n.2223G>T
XM_005272162.3:c.912G>T	XP_005272219.1:p.Val304=
XM_006716932.2:c.1758G>T	XP_006716995.1:p.Val586=
XM_011518140.2:c.1962G>T	XP_011516442.1:p.Val654=
XM_011518141.2:c.1896G>T	XP_011516443.1:p.Val632=
XM_011518142.2:c.1800G>T	XP_011516444.1:p.Val600=
XM_011518143.2:c.1794G>T	XP_011516445.1:p.Val598=
XM_011518145.2:c.1653G>T	XP_011516447.1:p.Val551=
XM_017014205.2:c.912G>T	XP_016869694.1:p.Val304=
XM_024447380.1:c.912G>T	XP_024303148.1:p.Val304=
XM_024447381.1:c.1218G>T	XP_024303149.1:p.Val406=
XM_024447382.1:c.912G>T	XP_024303150.1:p.Val304=
XR_001746160.2:n.2213G>T
XR_001746162.2:n.2418G>T
XR_001746164.1:n.2135G>T
XR_001746166.2:n.2430G>T
NM_001077365.2:c.2043G>T MANE Select	NP_001070833.1:p.Val681=
NM_001077366.2:c.1881G>T	NP_001070834.1:p.Val627=
NM_001136113.2:c.2043G>T	NP_001129585.1:p.Val681=
NM_001136114.2:c.1692G>T	NP_001129586.1:p.Val564=
NM_001353193.2:c.2109G>T	NP_001340122.2:p.Val703=
NM_001353194.2:c.1881G>T	NP_001340123.1:p.Val627=
NM_001353195.2:c.1692G>T	NP_001340124.1:p.Val564=
NM_001353196.2:c.1953G>T	NP_001340125.1:p.Val651=
NM_001353197.2:c.1947G>T	NP_001340126.2:p.Val649=
NM_001353198.2:c.1947G>T	NP_001340127.2:p.Val649=
NM_001353199.2:c.1758G>T	NP_001340128.2:p.Val586=
NM_001353200.2:c.1587G>T	NP_001340129.1:p.Val529=
NM_001374689.1:c.2031G>T	NP_001361618.1:p.Val677=
NM_001374690.1:c.1824G>T	NP_001361619.1:p.Val608=
NM_001374691.1:c.1692G>T	NP_001361620.1:p.Val564=
NM_001374692.1:c.1692G>T	NP_001361621.1:p.Val564=
NM_001374693.1:c.1692G>T	NP_001361622.1:p.Val564=
NM_001374695.1:c.1653G>T	NP_001361624.1:p.Val551=
NM_007171.4:c.2109G>T	NP_009102.4:p.Val703=
NR_148391.2:n.2077G>T
NR_148392.2:n.2295G>T
NR_148393.2:n.2216G>T
NR_148394.2:n.1970G>T
NR_148395.2:n.2368G>T
NR_148396.2:n.2002G>T
NR_148397.2:n.2127G>T
NR_148398.2:n.2082G>T
NR_148399.2:n.2608G>T
NR_148400.2:n.2207G>T