Canonical Allele Identifier: CA413848850

Gene: COL4A6

Linked Data

• MyVariant Identifiers: chrX:g.107400481C>A (hg19) ; chrX:g.108157251C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108157251C>A , CM000685.2:g.108157251C>A	GRCh38
NC_000023.10:g.107400481C>A , CM000685.1:g.107400481C>A	GRCh37
NC_000023.9:g.107287137C>A	NCBI36
NG_012059.2:g.287224G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334504.12:c.4822G>T MANE Select	ENSP00000334733.7:p.Ala1608Ser
ENST00000334504.11:c.4822G>T	ENSP00000334733.7:p.Ala1608Ser
ENST00000372216.8:c.4825G>T	ENSP00000361290.4:p.Ala1609Ser
ENST00000394872.6:c.4873G>T	ENSP00000378340.3:p.Ala1625Ser
ENST00000538570.5:c.4651G>T	ENSP00000445236.1:p.Ala1551Ser
ENST00000545689.2:c.4786G>T	ENSP00000443707.2:p.Ala1596Ser
ENST00000621266.4:c.4750G>T	ENSP00000482970.1:p.Ala1584Ser
NM_001287758.1:c.4873G>T	NP_001274687.1:p.Ala1625Ser
NM_001287759.1:c.4750G>T	NP_001274688.1:p.Ala1584Ser
NM_001287760.1:c.4651G>T	NP_001274689.1:p.Ala1551Ser
NM_001847.3:c.4825G>T	NP_001838.2:p.Ala1609Ser
NM_033641.3:c.4822G>T	NP_378667.1:p.Ala1608Ser
XM_006724617.2:c.4876G>T	XP_006724680.1:p.Ala1626Ser
XM_011530852.1:c.4804G>T	XP_011529154.1:p.Ala1602Ser
XM_011530853.1:c.4792G>T	XP_011529155.1:p.Ala1598Ser
XM_006724617.3:c.4876G>T	XP_006724680.1:p.Ala1626Ser
XM_011530852.2:c.4804G>T	XP_011529154.1:p.Ala1602Ser
XM_011530853.3:c.4792G>T	XP_011529155.1:p.Ala1598Ser
NM_001847.4:c.4825G>T	NP_001838.2:p.Ala1609Ser
NM_033641.4:c.4822G>T MANE Select	NP_378667.1:p.Ala1608Ser
NM_001287758.2:c.4873G>T	NP_001274687.1:p.Ala1625Ser
NM_001287759.2:c.4750G>T	NP_001274688.1:p.Ala1584Ser
NM_001287760.2:c.4651G>T	NP_001274689.1:p.Ala1551Ser