Canonical Allele Identifier: CA413848528

Gene: COL4A6

Linked Data

• MyVariant Identifiers: chrX:g.107400427C>A (hg19) ; chrX:g.108157197C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108157197C>A , CM000685.2:g.108157197C>A	GRCh38
NC_000023.10:g.107400427C>A , CM000685.1:g.107400427C>A	GRCh37
NC_000023.9:g.107287083C>A	NCBI36
NG_012059.2:g.287278G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334504.12:c.4876G>T MANE Select	ENSP00000334733.7:p.Asp1626Tyr
ENST00000334504.11:c.4876G>T	ENSP00000334733.7:p.Asp1626Tyr
ENST00000372216.8:c.4879G>T	ENSP00000361290.4:p.Asp1627Tyr
ENST00000394872.6:c.4927G>T	ENSP00000378340.3:p.Asp1643Tyr
ENST00000538570.5:c.4705G>T	ENSP00000445236.1:p.Asp1569Tyr
ENST00000545689.2:c.4840G>T	ENSP00000443707.2:p.Asp1614Tyr
ENST00000621266.4:c.4804G>T	ENSP00000482970.1:p.Asp1602Tyr
NM_001287758.1:c.4927G>T	NP_001274687.1:p.Asp1643Tyr
NM_001287759.1:c.4804G>T	NP_001274688.1:p.Asp1602Tyr
NM_001287760.1:c.4705G>T	NP_001274689.1:p.Asp1569Tyr
NM_001847.3:c.4879G>T	NP_001838.2:p.Asp1627Tyr
NM_033641.3:c.4876G>T	NP_378667.1:p.Asp1626Tyr
XM_006724617.2:c.4930G>T	XP_006724680.1:p.Asp1644Tyr
XM_011530852.1:c.4858G>T	XP_011529154.1:p.Asp1620Tyr
XM_011530853.1:c.4846G>T	XP_011529155.1:p.Asp1616Tyr
XM_006724617.3:c.4930G>T	XP_006724680.1:p.Asp1644Tyr
XM_011530852.2:c.4858G>T	XP_011529154.1:p.Asp1620Tyr
XM_011530853.3:c.4846G>T	XP_011529155.1:p.Asp1616Tyr
NM_001847.4:c.4879G>T	NP_001838.2:p.Asp1627Tyr
NM_033641.4:c.4876G>T MANE Select	NP_378667.1:p.Asp1626Tyr
NM_001287758.2:c.4927G>T	NP_001274687.1:p.Asp1643Tyr
NM_001287759.2:c.4804G>T	NP_001274688.1:p.Asp1602Tyr
NM_001287760.2:c.4705G>T	NP_001274689.1:p.Asp1569Tyr