Canonical Allele Identifier: CA518100881

Gene: COL4A6

Linked Data

• MyVariant Identifiers: chrX:g.107400467A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108157237A>C , CM000685.2:g.108157237A>C	GRCh38
NC_000023.10:g.107400467A>C , CM000685.1:g.107400467A>C	GRCh37
NC_000023.9:g.107287123A>C	NCBI36
NG_012059.2:g.287238T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334504.12:c.4836T>G MANE Select	ENSP00000334733.7:p.Gly1612=
ENST00000334504.11:c.4836T>G	ENSP00000334733.7:p.Gly1612=
ENST00000372216.8:c.4839T>G	ENSP00000361290.4:p.Gly1613=
ENST00000394872.6:c.4887T>G	ENSP00000378340.3:p.Gly1629=
ENST00000538570.5:c.4665T>G	ENSP00000445236.1:p.Gly1555=
ENST00000545689.2:c.4800T>G	ENSP00000443707.2:p.Gly1600=
ENST00000621266.4:c.4764T>G	ENSP00000482970.1:p.Gly1588=
NM_001287758.1:c.4887T>G	NP_001274687.1:p.Gly1629=
NM_001287759.1:c.4764T>G	NP_001274688.1:p.Gly1588=
NM_001287760.1:c.4665T>G	NP_001274689.1:p.Gly1555=
NM_001847.3:c.4839T>G	NP_001838.2:p.Gly1613=
NM_033641.3:c.4836T>G	NP_378667.1:p.Gly1612=
XM_006724617.2:c.4890T>G	XP_006724680.1:p.Gly1630=
XM_011530852.1:c.4818T>G	XP_011529154.1:p.Gly1606=
XM_011530853.1:c.4806T>G	XP_011529155.1:p.Gly1602=
XM_006724617.3:c.4890T>G	XP_006724680.1:p.Gly1630=
XM_011530852.2:c.4818T>G	XP_011529154.1:p.Gly1606=
XM_011530853.3:c.4806T>G	XP_011529155.1:p.Gly1602=
NM_001847.4:c.4839T>G	NP_001838.2:p.Gly1613=
NM_033641.4:c.4836T>G MANE Select	NP_378667.1:p.Gly1612=
NM_001287758.2:c.4887T>G	NP_001274687.1:p.Gly1629=
NM_001287759.2:c.4764T>G	NP_001274688.1:p.Gly1588=
NM_001287760.2:c.4665T>G	NP_001274689.1:p.Gly1555=