Canonical Allele Identifier: CA2148327487
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278473A= , CM000676.2:g.77278473A= GRCh38
NC_000014.8:g.77744816A= , CM000676.1:g.77744816A= GRCh37
NC_000014.7:g.76814569A= NCBI36
NG_008897.1:g.47410T= , LRG_844:g.47410T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.993T=
ENST00000556394.2:c.1609T= ENSP00000451967.2:p.Trp537=
ENST00000682247.1:c.2057T= ENSP00000507213.1:p.Leu686=
ENST00000682395.1:n.2532T=
ENST00000682459.1:n.1771T=
ENST00000682467.1:c.1927T= ENSP00000508062.1:p.Trp643=
ENST00000682795.1:c.2215T= ENSP00000507574.1:p.Trp739=
ENST00000682895.1:n.1784T=
ENST00000682955.1:n.1642T=
ENST00000683188.1:c.2329T=
ENST00000683380.1:n.1732T=
ENST00000683907.1:c.333T= ENSP00000507754.1:n.333T=
ENST00000684259.1:n.3835T=
ENST00000684538.1:n.1447T=
ENST00000684549.1:n.1619T=
ENST00000261534.9:c.2068T= MANE Select ENSP00000261534.4:p.Trp690=
ENST00000261534.8:c.2068T= ENSP00000261534.4:p.Trp690=
ENST00000452340.7:n.3044T=
ENST00000554767.5:n.2854T=
ENST00000555710.1:c.429T= ENSP00000451730.1:n.429T=
ENST00000556394.1:c.123T=
ENST00000556446.1:n.369T=
ENST00000602717.5:c.283T= ENSP00000487704.1:p.Trp95=
NM_013382.5:c.2068T= , LRG_844t1:c.2068T= NP_037514.2:p.Trp690=
XM_011536675.1:c.2257T= XP_011534977.1:p.Trp753=
XM_011536676.1:c.1924T= XP_011534978.1:p.Trp642=
XM_011536677.1:c.1798T= XP_011534979.1:p.Trp600=
XM_011536679.1:c.1351T= XP_011534981.1:p.Trp451=
XR_943416.1:n.2321T=
XM_011536675.2:c.2257T= XP_011534977.1:p.Trp753=
XM_011536676.2:c.1924T= XP_011534978.1:p.Trp642=
XM_011536677.3:c.1798T= XP_011534979.1:p.Trp600=
XR_001750279.1:n.2354T=
XR_001750282.1:n.3007T=
XR_943416.3:n.2319T=
NM_013382.6:c.2068T= NP_037514.2:p.Trp690=
NM_013382.7:c.2068T= MANE Select NP_037514.2:p.Trp690=