Canonical Allele Identifier: CA258567
Gene: COL4A5 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 24458
ClinVar RCV Id: RCV000021337
dbSNP Id: rs104886145

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108598817G>A , CM000685.2:g.108598817G>A GRCh38
NC_000023.10:g.107842047G>A , CM000685.1:g.107842047G>A GRCh37
NC_000023.9:g.107728703G>A NCBI36
NG_011977.1:g.163894G>A
NG_011977.2:g.163894G>A

Transcript Alleles

HGVS Amino-acid change
NM_000495.4:c.1895G>A VV NP_000486.1:p.Gly632Asp
NM_033380.2:c.1895G>A VV NP_203699.1:p.Gly632Asp
XM_005262070.2:c.1895G>A XP_005262127.1:p.Gly632Asp
XM_005262072.3:c.1895G>A XP_005262129.1:p.Gly632Asp
XM_006724616.2:c.1895G>A XP_006724679.1:p.Gly632Asp
XM_011530849.1:c.1571G>A XP_011529151.1:p.Gly524Asp
XM_011530850.1:c.1895G>A XP_011529152.1:p.Gly632Asp
XM_011530849.2:c.1910G>A XP_011529151.2:p.Gly637Asp
XM_017029259.2:c.1910G>A XP_016884748.1:p.Gly637Asp
XM_017029260.1:c.1910G>A XP_016884749.1:p.Gly637Asp
XM_017029261.1:c.1910G>A XP_016884750.1:p.Gly637Asp
XM_017029262.2:c.1910G>A XP_016884751.1:p.Gly637Asp
XM_017029263.2:c.230G>A XP_016884752.1:p.Gly77Asp
ENST00000328300.10:c.1895G>A ENSP00000331902.6:p.Gly632Asp
ENST00000361603.6:c.1895G>A ENSP00000354505.2:p.Gly632Asp
ENST00000483338.1:n.1351G>A