Canonical Allele Identifier: CA1332795963
Gene: COL4A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227164647A= , CM000664.2:g.227164647A= GRCh38
NC_000002.11:g.228029363A= , CM000664.1:g.228029363A= GRCh37
NC_000002.10:g.227737607A= NCBI36
NG_011591.1:g.5083A= , LRG_230:g.5083A=
NG_011592.1:g.4913T= , LRG_231:g.4913T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396578.8:c.-80A= MANE Select ENSP00000379823.3:n.-80A=
ENST00000396578.7:c.-80A= ENSP00000379823.3:n.-80A=
NM_000091.4:c.-80A= , LRG_230t1:c.-80A= NP_000082.2:n.-80A=
XM_005246276.2:c.-80A= XP_005246333.1:n.-80A=
XM_005246277.2:c.-80A= XP_005246334.1:n.-80A=
XM_005246280.2:c.-80A= XP_005246337.1:n.-80A=
XM_006712245.2:c.-80A= XP_006712308.1:n.-80A=
XM_011510555.1:c.-80A= XP_011508857.1:n.-80A=
XR_241280.2:n.59A=
XM_005246277.3:c.-80A= XP_005246334.1:n.-80A=
XM_005246280.3:c.-80A= XP_005246337.1:n.-80A=
XM_006712245.3:c.-80A= XP_006712308.1:n.-80A=
XM_017003295.1:c.-80A= XP_016858784.1:n.-80A=
XR_001738601.1:n.59A=
XR_241280.3:n.59A=
NM_000091.5:c.-80A= MANE Select NP_000082.2:n.-80A=