Canonical Allele Identifier: CA390520291

Gene: POMT2

Linked Data

• gnomAD v4: 14-77301193-C-T
• MyVariant Identifiers: chr14:g.77767536C>T (hg19) ; chr14:g.77301193C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77301193C>T , CM000676.2:g.77301193C>T	GRCh38
NC_000014.8:g.77767536C>T , CM000676.1:g.77767536C>T	GRCh37
NC_000014.7:g.76837289C>T	NCBI36
NG_008897.1:g.24690G>A , LRG_844:g.24690G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553863.6:c.166G>A	ENSP00000508202.1:n.166G>A
ENST00000556394.2:c.358-1632G>A	ENSP00000451967.2:n.358-1632G>A
ENST00000556880.6:n.737G>A
ENST00000557289.2:c.57G>A
ENST00000682247.1:c.713G>A	ENSP00000507213.1:p.Gly238Asp
ENST00000682382.1:c.496-2422G>A
ENST00000682395.1:n.442G>A
ENST00000682459.1:n.377G>A
ENST00000682467.1:c.713G>A	ENSP00000508062.1:p.Gly238Asp
ENST00000682795.1:c.713G>A	ENSP00000507574.1:p.Gly238Asp
ENST00000682895.1:n.429G>A
ENST00000682955.1:n.212-2422G>A
ENST00000683167.1:c.57G>A
ENST00000683188.1:c.343-1632G>A
ENST00000683300.1:c.109+3499G>A	ENSP00000507630.1:n.109+3499G>A
ENST00000683328.1:c.109+3499G>A	ENSP00000508096.1:n.109+3499G>A
ENST00000683380.1:n.377G>A
ENST00000683398.1:c.57G>A
ENST00000683551.1:c.109+1642G>A
ENST00000683828.1:c.526-1632G>A
ENST00000684259.1:n.564G>A
ENST00000684549.1:n.368-1632G>A
ENST00000684554.1:c.57G>A
ENST00000261534.9:c.713G>A MANE Select	ENSP00000261534.4:p.Gly238Asp
ENST00000261534.8:c.713G>A	ENSP00000261534.4:p.Gly238Asp
ENST00000452340.7:n.736G>A
ENST00000553863.5:n.377G>A
ENST00000555675.5:n.429G>A
ENST00000556326.5:c.*379G>A	ENSP00000450630.1:n.*379G>A
ENST00000557289.1:c.56-1632G>A	ENSP00000451115.1:n.56-1632G>A
NM_013382.5:c.713G>A , LRG_844t1:c.713G>A	NP_037514.2:p.Gly238Asp
XM_011536675.1:c.713G>A	XP_011534977.1:p.Gly238Asp
XM_011536676.1:c.380G>A	XP_011534978.1:p.Gly127Asp
XM_011536677.1:c.547+3499G>A	XP_011534979.1:n.547+3499G>A
XM_011536678.1:c.713G>A	XP_011534980.1:p.Gly238Asp
XM_011536679.1:c.-90-1632G>A	XP_011534981.1:n.-90-1632G>A
XM_011536680.1:c.713G>A	XP_011534982.1:p.Gly238Asp
XR_943416.1:n.916G>A
XM_011536675.2:c.713G>A	XP_011534977.1:p.Gly238Asp
XM_011536676.2:c.380G>A	XP_011534978.1:p.Gly127Asp
XM_011536677.3:c.547+3499G>A	XP_011534979.1:n.547+3499G>A
XR_001750279.1:n.913G>A
XR_001750282.1:n.917G>A
XR_943416.3:n.914G>A
NM_013382.6:c.713G>A	NP_037514.2:p.Gly238Asp
NM_013382.7:c.713G>A MANE Select	NP_037514.2:p.Gly238Asp