Canonical Allele Identifier: CA390520912

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77772682C>T (hg19) ; chr14:g.77306339C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77306339C>T , CM000676.2:g.77306339C>T	GRCh38
NC_000014.8:g.77772682C>T , CM000676.1:g.77772682C>T	GRCh37
NC_000014.7:g.76842435C>T	NCBI36
NG_008897.1:g.19544G>A , LRG_844:g.19544G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555675.6:n.165G>A
ENST00000556394.2:c.249-1539G>A	ENSP00000451967.2:n.249-1539G>A
ENST00000556880.6:n.369G>A
ENST00000682247.1:c.436G>A	ENSP00000507213.1:p.Gly146Arg
ENST00000682382.1:c.384G>A
ENST00000682395.1:n.165G>A
ENST00000682459.1:n.102+63G>A
ENST00000682467.1:c.436G>A	ENSP00000508062.1:p.Gly146Arg
ENST00000682795.1:c.436G>A	ENSP00000507574.1:p.Gly146Arg
ENST00000682895.1:n.152G>A
ENST00000682955.1:n.102+63G>A
ENST00000683188.1:c.231G>A
ENST00000683380.1:n.102+63G>A
ENST00000683828.1:c.305G>A
ENST00000684066.1:n.131G>A
ENST00000684102.1:n.182G>A
ENST00000684259.1:n.287G>A
ENST00000684479.1:n.103G>A
ENST00000684549.1:n.165G>A
ENST00000684600.1:c.250G>A
ENST00000684670.1:n.103G>A
ENST00000684746.1:n.133G>A
ENST00000261534.9:c.436G>A MANE Select	ENSP00000261534.4:p.Gly146Arg
ENST00000261534.8:c.436G>A	ENSP00000261534.4:p.Gly146Arg
ENST00000452340.7:n.459G>A
ENST00000553863.5:n.102+63G>A
ENST00000554948.1:c.163G>A	ENSP00000452060.1:p.Gly55Arg
ENST00000555675.5:n.152G>A
ENST00000555788.5:n.270G>A
ENST00000556326.5:c.*102G>A	ENSP00000450630.1:n.*102G>A
ENST00000556880.5:n.369G>A
ENST00000557525.1:n.526G>A
NM_013382.5:c.436G>A , LRG_844t1:c.436G>A	NP_037514.2:p.Gly146Arg
XM_011536675.1:c.436G>A	XP_011534977.1:p.Gly146Arg
XM_011536676.1:c.103G>A	XP_011534978.1:p.Gly35Arg
XM_011536677.1:c.436G>A	XP_011534979.1:p.Gly146Arg
XM_011536678.1:c.436G>A	XP_011534980.1:p.Gly146Arg
XM_011536680.1:c.436G>A	XP_011534982.1:p.Gly146Arg
XR_943416.1:n.639G>A
XM_011536675.2:c.436G>A	XP_011534977.1:p.Gly146Arg
XM_011536676.2:c.103G>A	XP_011534978.1:p.Gly35Arg
XM_011536677.3:c.436G>A	XP_011534979.1:p.Gly146Arg
XR_001750279.1:n.636G>A
XR_001750282.1:n.640G>A
XR_943416.3:n.637G>A
NM_013382.6:c.436G>A	NP_037514.2:p.Gly146Arg
NM_013382.7:c.436G>A MANE Select	NP_037514.2:p.Gly146Arg