Canonical Allele Identifier: CA413848669

Gene: COL4A6

Linked Data

• MyVariant Identifiers: chrX:g.107400451C>A (hg19) ; chrX:g.108157221C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108157221C>A , CM000685.2:g.108157221C>A	GRCh38
NC_000023.10:g.107400451C>A , CM000685.1:g.107400451C>A	GRCh37
NC_000023.9:g.107287107C>A	NCBI36
NG_012059.2:g.287254G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334504.12:c.4852G>T MANE Select	ENSP00000334733.7:p.Val1618Phe
ENST00000334504.11:c.4852G>T	ENSP00000334733.7:p.Val1618Phe
ENST00000372216.8:c.4855G>T	ENSP00000361290.4:p.Val1619Phe
ENST00000394872.6:c.4903G>T	ENSP00000378340.3:p.Val1635Phe
ENST00000538570.5:c.4681G>T	ENSP00000445236.1:p.Val1561Phe
ENST00000545689.2:c.4816G>T	ENSP00000443707.2:p.Val1606Phe
ENST00000621266.4:c.4780G>T	ENSP00000482970.1:p.Val1594Phe
NM_001287758.1:c.4903G>T	NP_001274687.1:p.Val1635Phe
NM_001287759.1:c.4780G>T	NP_001274688.1:p.Val1594Phe
NM_001287760.1:c.4681G>T	NP_001274689.1:p.Val1561Phe
NM_001847.3:c.4855G>T	NP_001838.2:p.Val1619Phe
NM_033641.3:c.4852G>T	NP_378667.1:p.Val1618Phe
XM_006724617.2:c.4906G>T	XP_006724680.1:p.Val1636Phe
XM_011530852.1:c.4834G>T	XP_011529154.1:p.Val1612Phe
XM_011530853.1:c.4822G>T	XP_011529155.1:p.Val1608Phe
XM_006724617.3:c.4906G>T	XP_006724680.1:p.Val1636Phe
XM_011530852.2:c.4834G>T	XP_011529154.1:p.Val1612Phe
XM_011530853.3:c.4822G>T	XP_011529155.1:p.Val1608Phe
NM_001847.4:c.4855G>T	NP_001838.2:p.Val1619Phe
NM_033641.4:c.4852G>T MANE Select	NP_378667.1:p.Val1618Phe
NM_001287758.2:c.4903G>T	NP_001274687.1:p.Val1635Phe
NM_001287759.2:c.4780G>T	NP_001274688.1:p.Val1594Phe
NM_001287760.2:c.4681G>T	NP_001274689.1:p.Val1561Phe