Canonical Allele Identifier: CA255268
Gene: COL4A5 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 10465
ClinVar RCV Id: RCV000011211
dbSNP Id: rs104886043

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108559083G>A , CM000685.2:g.108559083G>A GRCh38
NC_000023.10:g.107802313G>A , CM000685.1:g.107802313G>A GRCh37
NC_000023.9:g.107688969G>A NCBI36
NG_011977.1:g.124160G>A
NG_011977.2:g.124160G>A

Transcript Alleles

HGVS Amino-acid change
NM_000495.4:c.161G>A VV NP_000486.1:p.Gly54Asp
NM_033380.2:c.161G>A VV NP_203699.1:p.Gly54Asp
XM_005262070.2:c.161G>A XP_005262127.1:p.Gly54Asp
XM_005262072.3:c.161G>A XP_005262129.1:p.Gly54Asp
XM_006724616.2:c.161G>A XP_006724679.1:p.Gly54Asp
XM_011530849.1:c.-164G>A XP_011529151.1:p.=
XM_011530850.1:c.161G>A XP_011529152.1:p.Gly54Asp
XM_011530849.2:c.176G>A XP_011529151.2:p.Gly59Asp
XM_017029259.2:c.176G>A XP_016884748.1:p.Gly59Asp
XM_017029260.1:c.176G>A XP_016884749.1:p.Gly59Asp
XM_017029261.1:c.176G>A XP_016884750.1:p.Gly59Asp
XM_017029262.2:c.176G>A XP_016884751.1:p.Gly59Asp
ENST00000328300.10:c.161G>A ENSP00000331902.6:p.Gly54Asp
ENST00000361603.6:c.161G>A ENSP00000354505.2:p.Gly54Asp
ENST00000470339.1:n.345G>A