Canonical Allele Identifier: CA413848494

Gene: COL4A6

Linked Data

• dbSNP Id: rs1377459124
• MyVariant Identifiers: chrX:g.107400418C>T (hg19) ; chrX:g.108157188C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108157188C>T , CM000685.2:g.108157188C>T	GRCh38
NC_000023.10:g.107400418C>T , CM000685.1:g.107400418C>T	GRCh37
NC_000023.9:g.107287074C>T	NCBI36
NG_012059.2:g.287287G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334504.12:c.4885G>A MANE Select	ENSP00000334733.7:p.Ala1629Thr
ENST00000334504.11:c.4885G>A	ENSP00000334733.7:p.Ala1629Thr
ENST00000372216.8:c.4888G>A	ENSP00000361290.4:p.Ala1630Thr
ENST00000394872.6:c.4936G>A	ENSP00000378340.3:p.Ala1646Thr
ENST00000538570.5:c.4714G>A	ENSP00000445236.1:p.Ala1572Thr
ENST00000545689.2:c.4849G>A	ENSP00000443707.2:p.Ala1617Thr
ENST00000621266.4:c.4813G>A	ENSP00000482970.1:p.Ala1605Thr
NM_001287758.1:c.4936G>A	NP_001274687.1:p.Ala1646Thr
NM_001287759.1:c.4813G>A	NP_001274688.1:p.Ala1605Thr
NM_001287760.1:c.4714G>A	NP_001274689.1:p.Ala1572Thr
NM_001847.3:c.4888G>A	NP_001838.2:p.Ala1630Thr
NM_033641.3:c.4885G>A	NP_378667.1:p.Ala1629Thr
XM_006724617.2:c.4939G>A	XP_006724680.1:p.Ala1647Thr
XM_011530852.1:c.4867G>A	XP_011529154.1:p.Ala1623Thr
XM_011530853.1:c.4855G>A	XP_011529155.1:p.Ala1619Thr
XM_006724617.3:c.4939G>A	XP_006724680.1:p.Ala1647Thr
XM_011530852.2:c.4867G>A	XP_011529154.1:p.Ala1623Thr
XM_011530853.3:c.4855G>A	XP_011529155.1:p.Ala1619Thr
NM_001847.4:c.4888G>A	NP_001838.2:p.Ala1630Thr
NM_033641.4:c.4885G>A MANE Select	NP_378667.1:p.Ala1629Thr
NM_001287758.2:c.4936G>A	NP_001274687.1:p.Ala1646Thr
NM_001287759.2:c.4813G>A	NP_001274688.1:p.Ala1605Thr
NM_001287760.2:c.4714G>A	NP_001274689.1:p.Ala1572Thr