Canonical Allele Identifier: CA413848728

Gene: COL4A6

Linked Data

• MyVariant Identifiers: chrX:g.107400459T>C (hg19) ; chrX:g.108157229T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108157229T>C , CM000685.2:g.108157229T>C	GRCh38
NC_000023.10:g.107400459T>C , CM000685.1:g.107400459T>C	GRCh37
NC_000023.9:g.107287115T>C	NCBI36
NG_012059.2:g.287246A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334504.12:c.4844A>G MANE Select	ENSP00000334733.7:p.Gln1615Arg
ENST00000334504.11:c.4844A>G	ENSP00000334733.7:p.Gln1615Arg
ENST00000372216.8:c.4847A>G	ENSP00000361290.4:p.Gln1616Arg
ENST00000394872.6:c.4895A>G	ENSP00000378340.3:p.Gln1632Arg
ENST00000538570.5:c.4673A>G	ENSP00000445236.1:p.Gln1558Arg
ENST00000545689.2:c.4808A>G	ENSP00000443707.2:p.Gln1603Arg
ENST00000621266.4:c.4772A>G	ENSP00000482970.1:p.Gln1591Arg
NM_001287758.1:c.4895A>G	NP_001274687.1:p.Gln1632Arg
NM_001287759.1:c.4772A>G	NP_001274688.1:p.Gln1591Arg
NM_001287760.1:c.4673A>G	NP_001274689.1:p.Gln1558Arg
NM_001847.3:c.4847A>G	NP_001838.2:p.Gln1616Arg
NM_033641.3:c.4844A>G	NP_378667.1:p.Gln1615Arg
XM_006724617.2:c.4898A>G	XP_006724680.1:p.Gln1633Arg
XM_011530852.1:c.4826A>G	XP_011529154.1:p.Gln1609Arg
XM_011530853.1:c.4814A>G	XP_011529155.1:p.Gln1605Arg
XM_006724617.3:c.4898A>G	XP_006724680.1:p.Gln1633Arg
XM_011530852.2:c.4826A>G	XP_011529154.1:p.Gln1609Arg
XM_011530853.3:c.4814A>G	XP_011529155.1:p.Gln1605Arg
NM_001847.4:c.4847A>G	NP_001838.2:p.Gln1616Arg
NM_033641.4:c.4844A>G MANE Select	NP_378667.1:p.Gln1615Arg
NM_001287758.2:c.4895A>G	NP_001274687.1:p.Gln1632Arg
NM_001287759.2:c.4772A>G	NP_001274688.1:p.Gln1591Arg
NM_001287760.2:c.4673A>G	NP_001274689.1:p.Gln1558Arg