Canonical Allele Identifier: CA66598974
Gene: COL4A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 447169
dbSNP Id: rs868002181

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227280970G>A , CM000664.2:g.227280970G>A GRCh38
NC_000002.11:g.228145686G>A , CM000664.1:g.228145686G>A GRCh37
NC_000002.10:g.227853930G>A NCBI36
NG_011591.1:g.121406G>A , LRG_230:g.121406G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000396578.8:c.2452G>A MANE Select ENSP00000379823.3:p.Gly818Arg
ENST00000396578.7:c.2452G>A ENSP00000379823.3:p.Gly818Arg
NM_000091.4:c.2452G>A , LRG_230t1:c.2452G>A NP_000082.2:p.Gly818Arg
NR_102371.1:n.329+734C>T
XM_005246276.2:c.2452G>A XP_005246333.1:p.Gly818Arg
XM_005246277.2:c.2347G>A XP_005246334.1:p.Gly783Arg
XM_005246280.2:c.2452G>A XP_005246337.1:p.Gly818Arg
XM_006712245.2:c.2452G>A XP_006712308.1:p.Gly818Arg
XM_011510555.1:c.2452G>A XP_011508857.1:p.Gly818Arg
XM_011510556.1:c.1213G>A XP_011508858.1:p.Gly405Arg
XR_241280.2:n.2590G>A
XM_005246277.3:c.2347G>A XP_005246334.1:p.Gly783Arg
XM_005246280.3:c.2452G>A XP_005246337.1:p.Gly818Arg
XM_006712245.3:c.2452G>A XP_006712308.1:p.Gly818Arg
XM_011510556.2:c.1213G>A XP_011508858.1:p.Gly405Arg
XM_017003295.1:c.2452G>A XP_016858784.1:p.Gly818Arg
XR_001738601.1:n.2590G>A
XR_241280.3:n.2590G>A
NM_000091.5:c.2452G>A MANE Select NP_000082.2:p.Gly818Arg