Canonical Allele Identifier: CA10487100
Gene: COL4A6 HGNC NCBI

Linked Data

dbSNP Id: rs767479071

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108157232C>T , CM000685.2:g.108157232C>T GRCh38
NC_000023.10:g.107400462C>T , CM000685.1:g.107400462C>T GRCh37
NC_000023.9:g.107287118C>T NCBI36
NG_012059.2:g.287243G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000334504.12:c.4841G>A MANE Select ENSP00000334733.7:p.Gly1614Asp
ENST00000334504.11:c.4841G>A ENSP00000334733.7:p.Gly1614Asp
ENST00000372216.8:c.4844G>A ENSP00000361290.4:p.Gly1615Asp
ENST00000394872.6:c.4892G>A ENSP00000378340.3:p.Gly1631Asp
ENST00000538570.5:c.4670G>A ENSP00000445236.1:p.Gly1557Asp
ENST00000545689.2:c.4805G>A ENSP00000443707.2:p.Gly1602Asp
ENST00000621266.4:c.4769G>A ENSP00000482970.1:p.Gly1590Asp
NM_001287758.1:c.4892G>A NP_001274687.1:p.Gly1631Asp
NM_001287759.1:c.4769G>A NP_001274688.1:p.Gly1590Asp
NM_001287760.1:c.4670G>A NP_001274689.1:p.Gly1557Asp
NM_001847.3:c.4844G>A NP_001838.2:p.Gly1615Asp
NM_033641.3:c.4841G>A NP_378667.1:p.Gly1614Asp
XM_006724617.2:c.4895G>A XP_006724680.1:p.Gly1632Asp
XM_011530852.1:c.4823G>A XP_011529154.1:p.Gly1608Asp
XM_011530853.1:c.4811G>A XP_011529155.1:p.Gly1604Asp
XM_006724617.3:c.4895G>A XP_006724680.1:p.Gly1632Asp
XM_011530852.2:c.4823G>A XP_011529154.1:p.Gly1608Asp
XM_011530853.3:c.4811G>A XP_011529155.1:p.Gly1604Asp
NM_001847.4:c.4844G>A NP_001838.2:p.Gly1615Asp
NM_033641.4:c.4841G>A MANE Select NP_378667.1:p.Gly1614Asp
NM_001287758.2:c.4892G>A NP_001274687.1:p.Gly1631Asp
NM_001287759.2:c.4769G>A NP_001274688.1:p.Gly1590Asp
NM_001287760.2:c.4670G>A NP_001274689.1:p.Gly1557Asp