Canonical Allele Identifier: CA10487315

Gene: COL4A6

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108165024C>T , CM000685.2:g.108165024C>T	GRCh38
NC_000023.10:g.107408254C>T , CM000685.1:g.107408254C>T	GRCh37
NC_000023.9:g.107294910C>T	NCBI36
NG_012059.2:g.279451G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334504.12:c.3823G>A MANE Select	ENSP00000334733.7:p.Ala1275Thr
ENST00000334504.11:c.3823G>A	ENSP00000334733.7:p.Ala1275Thr
ENST00000372216.8:c.3826G>A	ENSP00000361290.4:p.Ala1276Thr
ENST00000394872.6:c.3874G>A	ENSP00000378340.3:p.Ala1292Thr
ENST00000538570.5:c.3751G>A	ENSP00000445236.1:p.Ala1251Thr
ENST00000545689.2:c.3823G>A	ENSP00000443707.2:p.Ala1275Thr
ENST00000621266.4:c.3751G>A	ENSP00000482970.1:p.Ala1251Thr
NM_001287758.1:c.3874G>A	NP_001274687.1:p.Ala1292Thr
NM_001287759.1:c.3751G>A	NP_001274688.1:p.Ala1251Thr
NM_001287760.1:c.3751G>A	NP_001274689.1:p.Ala1251Thr
NM_001847.3:c.3826G>A	NP_001838.2:p.Ala1276Thr
NM_033641.3:c.3823G>A	NP_378667.1:p.Ala1275Thr
XM_006724617.2:c.3877G>A	XP_006724680.1:p.Ala1293Thr
XM_011530852.1:c.3805G>A	XP_011529154.1:p.Ala1269Thr
XM_011530853.1:c.3793G>A	XP_011529155.1:p.Ala1265Thr
XM_006724617.3:c.3877G>A	XP_006724680.1:p.Ala1293Thr
XM_011530852.2:c.3805G>A	XP_011529154.1:p.Ala1269Thr
XM_011530853.3:c.3793G>A	XP_011529155.1:p.Ala1265Thr
NM_001847.4:c.3826G>A	NP_001838.2:p.Ala1276Thr
NM_033641.4:c.3823G>A MANE Select	NP_378667.1:p.Ala1275Thr
NM_001287758.2:c.3874G>A	NP_001274687.1:p.Ala1292Thr
NM_001287759.2:c.3751G>A	NP_001274688.1:p.Ala1251Thr
NM_001287760.2:c.3751G>A	NP_001274689.1:p.Ala1251Thr