Canonical Allele Identifier: CA390517671

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77753107G>C (hg19) ; chr14:g.77286764G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77286764G>C , CM000676.2:g.77286764G>C	GRCh38
NC_000014.8:g.77753107G>C , CM000676.1:g.77753107G>C	GRCh37
NC_000014.7:g.76822860G>C	NCBI36
NG_008897.1:g.39119C>G , LRG_844:g.39119C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556394.2:c.853C>G	ENSP00000451967.2:p.Gln285Glu
ENST00000682247.1:c.1312C>G	ENSP00000507213.1:p.Gln438Glu
ENST00000682382.1:c.884C>G
ENST00000682395.1:n.1490C>G
ENST00000682459.1:n.1015C>G
ENST00000682467.1:c.1312C>G	ENSP00000508062.1:p.Gln438Glu
ENST00000682706.1:n.89C>G
ENST00000682795.1:c.1312C>G	ENSP00000507574.1:p.Gln438Glu
ENST00000682895.1:n.1028C>G
ENST00000682955.1:n.600C>G
ENST00000683188.1:c.1287C>G
ENST00000683328.1:c.305C>G	ENSP00000508096.1:n.305C>G
ENST00000683380.1:n.976C>G
ENST00000683828.1:c.1021C>G
ENST00000684259.1:n.1163C>G
ENST00000684444.1:c.59C>G
ENST00000684549.1:n.863C>G
ENST00000261534.9:c.1312C>G MANE Select	ENSP00000261534.4:p.Gln438Glu
ENST00000261534.8:c.1312C>G	ENSP00000261534.4:p.Gln438Glu
ENST00000452340.7:n.1335C>G
ENST00000553880.5:n.183C>G
ENST00000554767.5:n.2098C>G
ENST00000554884.5:n.304C>G
ENST00000556404.1:n.446C>G
ENST00000556851.1:n.348C>G
ENST00000557675.5:n.402C>G
NM_013382.5:c.1312C>G , LRG_844t1:c.1312C>G	NP_037514.2:p.Gln438Glu
XM_011536675.1:c.1312C>G	XP_011534977.1:p.Gln438Glu
XM_011536676.1:c.979C>G	XP_011534978.1:p.Gln327Glu
XM_011536677.1:c.853C>G	XP_011534979.1:p.Gln285Glu
XM_011536678.1:c.1312C>G	XP_011534980.1:p.Gln438Glu
XM_011536679.1:c.406C>G	XP_011534981.1:p.Gln136Glu
XR_943416.1:n.1515C>G
XM_011536675.2:c.1312C>G	XP_011534977.1:p.Gln438Glu
XM_011536676.2:c.979C>G	XP_011534978.1:p.Gln327Glu
XM_011536677.3:c.853C>G	XP_011534979.1:p.Gln285Glu
XR_001750279.1:n.1512C>G
XR_001750282.1:n.1965C>G
XR_943416.3:n.1513C>G
NM_013382.6:c.1312C>G	NP_037514.2:p.Gln438Glu
NM_013382.7:c.1312C>G MANE Select	NP_037514.2:p.Gln438Glu