Canonical Allele Identifier: CA518100887

Gene: COL4A6

Linked Data

• MyVariant Identifiers: chrX:g.107400476A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108157246A>G , CM000685.2:g.108157246A>G	GRCh38
NC_000023.10:g.107400476A>G , CM000685.1:g.107400476A>G	GRCh37
NC_000023.9:g.107287132A>G	NCBI36
NG_012059.2:g.287229T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334504.12:c.4827T>C MANE Select	ENSP00000334733.7:p.Gly1609=
ENST00000334504.11:c.4827T>C	ENSP00000334733.7:p.Gly1609=
ENST00000372216.8:c.4830T>C	ENSP00000361290.4:p.Gly1610=
ENST00000394872.6:c.4878T>C	ENSP00000378340.3:p.Gly1626=
ENST00000538570.5:c.4656T>C	ENSP00000445236.1:p.Gly1552=
ENST00000545689.2:c.4791T>C	ENSP00000443707.2:p.Gly1597=
ENST00000621266.4:c.4755T>C	ENSP00000482970.1:p.Gly1585=
NM_001287758.1:c.4878T>C	NP_001274687.1:p.Gly1626=
NM_001287759.1:c.4755T>C	NP_001274688.1:p.Gly1585=
NM_001287760.1:c.4656T>C	NP_001274689.1:p.Gly1552=
NM_001847.3:c.4830T>C	NP_001838.2:p.Gly1610=
NM_033641.3:c.4827T>C	NP_378667.1:p.Gly1609=
XM_006724617.2:c.4881T>C	XP_006724680.1:p.Gly1627=
XM_011530852.1:c.4809T>C	XP_011529154.1:p.Gly1603=
XM_011530853.1:c.4797T>C	XP_011529155.1:p.Gly1599=
XM_006724617.3:c.4881T>C	XP_006724680.1:p.Gly1627=
XM_011530852.2:c.4809T>C	XP_011529154.1:p.Gly1603=
XM_011530853.3:c.4797T>C	XP_011529155.1:p.Gly1599=
NM_001847.4:c.4830T>C	NP_001838.2:p.Gly1610=
NM_033641.4:c.4827T>C MANE Select	NP_378667.1:p.Gly1609=
NM_001287758.2:c.4878T>C	NP_001274687.1:p.Gly1626=
NM_001287759.2:c.4755T>C	NP_001274688.1:p.Gly1585=
NM_001287760.2:c.4656T>C	NP_001274689.1:p.Gly1552=