Canonical Allele Identifier: CA258565
Gene: COL4A5 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 24457
ClinVar RCV Id: RCV000021336
dbSNP Id: rs104886144

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108598808G>A , CM000685.2:g.108598808G>A GRCh38
NC_000023.10:g.107842038G>A , CM000685.1:g.107842038G>A GRCh37
NC_000023.9:g.107728694G>A NCBI36
NG_011977.1:g.163885G>A
NG_011977.2:g.163885G>A

Transcript Alleles

HGVS Amino-acid change
NM_000495.4:c.1886G>A VV NP_000486.1:p.Gly629Asp
NM_033380.2:c.1886G>A VV NP_203699.1:p.Gly629Asp
XM_005262070.2:c.1886G>A XP_005262127.1:p.Gly629Asp
XM_005262072.3:c.1886G>A XP_005262129.1:p.Gly629Asp
XM_006724616.2:c.1886G>A XP_006724679.1:p.Gly629Asp
XM_011530849.1:c.1562G>A XP_011529151.1:p.Gly521Asp
XM_011530850.1:c.1886G>A XP_011529152.1:p.Gly629Asp
XM_011530849.2:c.1901G>A XP_011529151.2:p.Gly634Asp
XM_017029259.2:c.1901G>A XP_016884748.1:p.Gly634Asp
XM_017029260.1:c.1901G>A XP_016884749.1:p.Gly634Asp
XM_017029261.1:c.1901G>A XP_016884750.1:p.Gly634Asp
XM_017029262.2:c.1901G>A XP_016884751.1:p.Gly634Asp
XM_017029263.2:c.221G>A XP_016884752.1:p.Gly74Asp
ENST00000328300.10:c.1886G>A ENSP00000331902.6:p.Gly629Asp
ENST00000361603.6:c.1886G>A ENSP00000354505.2:p.Gly629Asp
ENST00000483338.1:n.1342G>A