Canonical Allele Identifier: CA518100761

Gene: COL4A6

Linked Data

• MyVariant Identifiers: chrX:g.107400335C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108157105C>A , CM000685.2:g.108157105C>A	GRCh38
NC_000023.10:g.107400335C>A , CM000685.1:g.107400335C>A	GRCh37
NC_000023.9:g.107286991C>A	NCBI36
NG_012059.2:g.287370G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334504.12:c.4968G>T MANE Select	ENSP00000334733.7:p.Val1656=
ENST00000334504.11:c.4968G>T	ENSP00000334733.7:p.Val1656=
ENST00000372216.8:c.4971G>T	ENSP00000361290.4:p.Val1657=
ENST00000394872.6:c.5019G>T	ENSP00000378340.3:p.Val1673=
ENST00000538570.5:c.4797G>T	ENSP00000445236.1:p.Val1599=
ENST00000545689.2:c.4932G>T	ENSP00000443707.2:p.Val1644=
ENST00000621266.4:c.4896G>T	ENSP00000482970.1:p.Val1632=
NM_001287758.1:c.5019G>T	NP_001274687.1:p.Val1673=
NM_001287759.1:c.4896G>T	NP_001274688.1:p.Val1632=
NM_001287760.1:c.4797G>T	NP_001274689.1:p.Val1599=
NM_001847.3:c.4971G>T	NP_001838.2:p.Val1657=
NM_033641.3:c.4968G>T	NP_378667.1:p.Val1656=
XM_006724617.2:c.5022G>T	XP_006724680.1:p.Val1674=
XM_011530852.1:c.4950G>T	XP_011529154.1:p.Val1650=
XM_011530853.1:c.4938G>T	XP_011529155.1:p.Val1646=
XM_006724617.3:c.5022G>T	XP_006724680.1:p.Val1674=
XM_011530852.2:c.4950G>T	XP_011529154.1:p.Val1650=
XM_011530853.3:c.4938G>T	XP_011529155.1:p.Val1646=
NM_001847.4:c.4971G>T	NP_001838.2:p.Val1657=
NM_033641.4:c.4968G>T MANE Select	NP_378667.1:p.Val1656=
NM_001287758.2:c.5019G>T	NP_001274687.1:p.Val1673=
NM_001287759.2:c.4896G>T	NP_001274688.1:p.Val1632=
NM_001287760.2:c.4797G>T	NP_001274689.1:p.Val1599=