Canonical Allele Identifier: CA2663415009
Gene: COL4A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227164685G>T , CM000664.2:g.227164685G>T GRCh38
NC_000002.11:g.228029401G>T , CM000664.1:g.228029401G>T GRCh37
NC_000002.10:g.227737645G>T NCBI36
NG_011591.1:g.5121G>T , LRG_230:g.5121G>T
NG_011592.1:g.4875C>A , LRG_231:g.4875C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000396578.8:c.-42G>T MANE Select ENSP00000379823.3:n.-42G>T
ENST00000396578.7:c.-42G>T ENSP00000379823.3:n.-42G>T
NM_000091.4:c.-42G>T , LRG_230t1:c.-42G>T NP_000082.2:n.-42G>T
XM_005246276.2:c.-42G>T XP_005246333.1:n.-42G>T
XM_005246277.2:c.-42G>T XP_005246334.1:n.-42G>T
XM_005246280.2:c.-42G>T XP_005246337.1:n.-42G>T
XM_006712245.2:c.-42G>T XP_006712308.1:n.-42G>T
XM_011510555.1:c.-42G>T XP_011508857.1:n.-42G>T
XR_241280.2:n.97G>T
XM_005246277.3:c.-42G>T XP_005246334.1:n.-42G>T
XM_005246280.3:c.-42G>T XP_005246337.1:n.-42G>T
XM_006712245.3:c.-42G>T XP_006712308.1:n.-42G>T
XM_017003295.1:c.-42G>T XP_016858784.1:n.-42G>T
XR_001738601.1:n.97G>T
XR_241280.3:n.97G>T
NM_000091.5:c.-42G>T MANE Select NP_000082.2:n.-42G>T