Canonical Allele Identifier: CA413848634

Gene: COL4A6

Linked Data

• MyVariant Identifiers: chrX:g.107400445G>C (hg19) ; chrX:g.108157215G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108157215G>C , CM000685.2:g.108157215G>C	GRCh38
NC_000023.10:g.107400445G>C , CM000685.1:g.107400445G>C	GRCh37
NC_000023.9:g.107287101G>C	NCBI36
NG_012059.2:g.287260C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334504.12:c.4858C>G MANE Select	ENSP00000334733.7:p.Pro1620Ala
ENST00000334504.11:c.4858C>G	ENSP00000334733.7:p.Pro1620Ala
ENST00000372216.8:c.4861C>G	ENSP00000361290.4:p.Pro1621Ala
ENST00000394872.6:c.4909C>G	ENSP00000378340.3:p.Pro1637Ala
ENST00000538570.5:c.4687C>G	ENSP00000445236.1:p.Pro1563Ala
ENST00000545689.2:c.4822C>G	ENSP00000443707.2:p.Pro1608Ala
ENST00000621266.4:c.4786C>G	ENSP00000482970.1:p.Pro1596Ala
NM_001287758.1:c.4909C>G	NP_001274687.1:p.Pro1637Ala
NM_001287759.1:c.4786C>G	NP_001274688.1:p.Pro1596Ala
NM_001287760.1:c.4687C>G	NP_001274689.1:p.Pro1563Ala
NM_001847.3:c.4861C>G	NP_001838.2:p.Pro1621Ala
NM_033641.3:c.4858C>G	NP_378667.1:p.Pro1620Ala
XM_006724617.2:c.4912C>G	XP_006724680.1:p.Pro1638Ala
XM_011530852.1:c.4840C>G	XP_011529154.1:p.Pro1614Ala
XM_011530853.1:c.4828C>G	XP_011529155.1:p.Pro1610Ala
XM_006724617.3:c.4912C>G	XP_006724680.1:p.Pro1638Ala
XM_011530852.2:c.4840C>G	XP_011529154.1:p.Pro1614Ala
XM_011530853.3:c.4828C>G	XP_011529155.1:p.Pro1610Ala
NM_001847.4:c.4861C>G	NP_001838.2:p.Pro1621Ala
NM_033641.4:c.4858C>G MANE Select	NP_378667.1:p.Pro1620Ala
NM_001287758.2:c.4909C>G	NP_001274687.1:p.Pro1637Ala
NM_001287759.2:c.4786C>G	NP_001274688.1:p.Pro1596Ala
NM_001287760.2:c.4687C>G	NP_001274689.1:p.Pro1563Ala