Canonical Allele Identifier: CA413848273

Gene: COL4A6

Linked Data

• MyVariant Identifiers: chrX:g.107400358A>C (hg19) ; chrX:g.108157128A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108157128A>C , CM000685.2:g.108157128A>C	GRCh38
NC_000023.10:g.107400358A>C , CM000685.1:g.107400358A>C	GRCh37
NC_000023.9:g.107287014A>C	NCBI36
NG_012059.2:g.287347T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334504.12:c.4945T>G MANE Select	ENSP00000334733.7:p.Tyr1649Asp
ENST00000334504.11:c.4945T>G	ENSP00000334733.7:p.Tyr1649Asp
ENST00000372216.8:c.4948T>G	ENSP00000361290.4:p.Tyr1650Asp
ENST00000394872.6:c.4996T>G	ENSP00000378340.3:p.Tyr1666Asp
ENST00000538570.5:c.4774T>G	ENSP00000445236.1:p.Tyr1592Asp
ENST00000545689.2:c.4909T>G	ENSP00000443707.2:p.Tyr1637Asp
ENST00000621266.4:c.4873T>G	ENSP00000482970.1:p.Tyr1625Asp
NM_001287758.1:c.4996T>G	NP_001274687.1:p.Tyr1666Asp
NM_001287759.1:c.4873T>G	NP_001274688.1:p.Tyr1625Asp
NM_001287760.1:c.4774T>G	NP_001274689.1:p.Tyr1592Asp
NM_001847.3:c.4948T>G	NP_001838.2:p.Tyr1650Asp
NM_033641.3:c.4945T>G	NP_378667.1:p.Tyr1649Asp
XM_006724617.2:c.4999T>G	XP_006724680.1:p.Tyr1667Asp
XM_011530852.1:c.4927T>G	XP_011529154.1:p.Tyr1643Asp
XM_011530853.1:c.4915T>G	XP_011529155.1:p.Tyr1639Asp
XM_006724617.3:c.4999T>G	XP_006724680.1:p.Tyr1667Asp
XM_011530852.2:c.4927T>G	XP_011529154.1:p.Tyr1643Asp
XM_011530853.3:c.4915T>G	XP_011529155.1:p.Tyr1639Asp
NM_001847.4:c.4948T>G	NP_001838.2:p.Tyr1650Asp
NM_033641.4:c.4945T>G MANE Select	NP_378667.1:p.Tyr1649Asp
NM_001287758.2:c.4996T>G	NP_001274687.1:p.Tyr1666Asp
NM_001287759.2:c.4873T>G	NP_001274688.1:p.Tyr1625Asp
NM_001287760.2:c.4774T>G	NP_001274689.1:p.Tyr1592Asp