Canonical Allele Identifier: CA390517654

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77753098C>A (hg19) ; chr14:g.77286755C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77286755C>A , CM000676.2:g.77286755C>A	GRCh38
NC_000014.8:g.77753098C>A , CM000676.1:g.77753098C>A	GRCh37
NC_000014.7:g.76822851C>A	NCBI36
NG_008897.1:g.39128G>T , LRG_844:g.39128G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556394.2:c.862G>T	ENSP00000451967.2:p.Gly288Cys
ENST00000682247.1:c.1321G>T	ENSP00000507213.1:p.Gly441Cys
ENST00000682382.1:c.893G>T
ENST00000682395.1:n.1499G>T
ENST00000682459.1:n.1024G>T
ENST00000682467.1:c.1321G>T	ENSP00000508062.1:p.Gly441Cys
ENST00000682706.1:n.98G>T
ENST00000682795.1:c.1321G>T	ENSP00000507574.1:p.Gly441Cys
ENST00000682895.1:n.1037G>T
ENST00000682955.1:n.609G>T
ENST00000683188.1:c.1296G>T
ENST00000683328.1:c.314G>T	ENSP00000508096.1:n.314G>T
ENST00000683380.1:n.985G>T
ENST00000683828.1:c.1030G>T
ENST00000684259.1:n.1172G>T
ENST00000684444.1:c.68G>T
ENST00000684549.1:n.872G>T
ENST00000261534.9:c.1321G>T MANE Select	ENSP00000261534.4:p.Gly441Cys
ENST00000261534.8:c.1321G>T	ENSP00000261534.4:p.Gly441Cys
ENST00000452340.7:n.1344G>T
ENST00000553880.5:n.192G>T
ENST00000554767.5:n.2107G>T
ENST00000554884.5:n.313G>T
ENST00000556404.1:n.455G>T
ENST00000556851.1:n.357G>T
ENST00000557675.5:n.411G>T
NM_013382.5:c.1321G>T , LRG_844t1:c.1321G>T	NP_037514.2:p.Gly441Cys
XM_011536675.1:c.1321G>T	XP_011534977.1:p.Gly441Cys
XM_011536676.1:c.988G>T	XP_011534978.1:p.Gly330Cys
XM_011536677.1:c.862G>T	XP_011534979.1:p.Gly288Cys
XM_011536678.1:c.1321G>T	XP_011534980.1:p.Gly441Cys
XM_011536679.1:c.415G>T	XP_011534981.1:p.Gly139Cys
XR_943416.1:n.1524G>T
XM_011536675.2:c.1321G>T	XP_011534977.1:p.Gly441Cys
XM_011536676.2:c.988G>T	XP_011534978.1:p.Gly330Cys
XM_011536677.3:c.862G>T	XP_011534979.1:p.Gly288Cys
XR_001750279.1:n.1521G>T
XR_001750282.1:n.1974G>T
XR_943416.3:n.1522G>T
NM_013382.6:c.1321G>T	NP_037514.2:p.Gly441Cys
NM_013382.7:c.1321G>T MANE Select	NP_037514.2:p.Gly441Cys