Canonical Allele Identifier: CA413848441

Gene: COL4A6

Linked Data

• MyVariant Identifiers: chrX:g.107400405A>G (hg19) ; chrX:g.108157175A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108157175A>G , CM000685.2:g.108157175A>G	GRCh38
NC_000023.10:g.107400405A>G , CM000685.1:g.107400405A>G	GRCh37
NC_000023.9:g.107287061A>G	NCBI36
NG_012059.2:g.287300T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334504.12:c.4898T>C MANE Select	ENSP00000334733.7:p.Ile1633Thr
ENST00000334504.11:c.4898T>C	ENSP00000334733.7:p.Ile1633Thr
ENST00000372216.8:c.4901T>C	ENSP00000361290.4:p.Ile1634Thr
ENST00000394872.6:c.4949T>C	ENSP00000378340.3:p.Ile1650Thr
ENST00000538570.5:c.4727T>C	ENSP00000445236.1:p.Ile1576Thr
ENST00000545689.2:c.4862T>C	ENSP00000443707.2:p.Ile1621Thr
ENST00000621266.4:c.4826T>C	ENSP00000482970.1:p.Ile1609Thr
NM_001287758.1:c.4949T>C	NP_001274687.1:p.Ile1650Thr
NM_001287759.1:c.4826T>C	NP_001274688.1:p.Ile1609Thr
NM_001287760.1:c.4727T>C	NP_001274689.1:p.Ile1576Thr
NM_001847.3:c.4901T>C	NP_001838.2:p.Ile1634Thr
NM_033641.3:c.4898T>C	NP_378667.1:p.Ile1633Thr
XM_006724617.2:c.4952T>C	XP_006724680.1:p.Ile1651Thr
XM_011530852.1:c.4880T>C	XP_011529154.1:p.Ile1627Thr
XM_011530853.1:c.4868T>C	XP_011529155.1:p.Ile1623Thr
XM_006724617.3:c.4952T>C	XP_006724680.1:p.Ile1651Thr
XM_011530852.2:c.4880T>C	XP_011529154.1:p.Ile1627Thr
XM_011530853.3:c.4868T>C	XP_011529155.1:p.Ile1623Thr
NM_001847.4:c.4901T>C	NP_001838.2:p.Ile1634Thr
NM_033641.4:c.4898T>C MANE Select	NP_378667.1:p.Ile1633Thr
NM_001287758.2:c.4949T>C	NP_001274687.1:p.Ile1650Thr
NM_001287759.2:c.4826T>C	NP_001274688.1:p.Ile1609Thr
NM_001287760.2:c.4727T>C	NP_001274689.1:p.Ile1576Thr