Canonical Allele Identifier: CA2146625
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

ClinVar Variation Id: 254979
dbSNP Id: rs11677877

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227266453A>G , CM000664.2:g.227266453A>G GRCh38
NC_000002.11:g.228131169A>G , CM000664.1:g.228131169A>G GRCh37
NC_000002.10:g.227839413A>G NCBI36
NG_011591.1:g.106889A>G , LRG_230:g.106889A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000396578.8:c.1352A>G (COL4A3) MANE Select ENSP00000379823.3:p.His451Arg
ENST00000396578.7:c.1352A>G (COL4A3) ENSP00000379823.3:p.His451Arg
NM_000091.4:c.1352A>G , LRG_230t1:c.1352A>G (COL4A3) NP_000082.2:p.His451Arg
NR_102371.1:n.656-518T>C (MFF-DT)
XM_005246276.2:c.1352A>G (COL4A3) XP_005246333.1:p.His451Arg
XM_005246277.2:c.1352A>G (COL4A3) XP_005246334.1:p.His451Arg
XM_005246280.2:c.1352A>G (COL4A3) XP_005246337.1:p.His451Arg
XM_006712245.2:c.1352A>G (COL4A3) XP_006712308.1:p.His451Arg
XM_011510555.1:c.1352A>G (COL4A3) XP_011508857.1:p.His451Arg
XM_011510556.1:c.113A>G (COL4A3) XP_011508858.1:p.His38Arg
XR_241280.2:n.1490A>G (COL4A3)
XM_005246277.3:c.1352A>G (COL4A3) XP_005246334.1:p.His451Arg
XM_005246280.3:c.1352A>G (COL4A3) XP_005246337.1:p.His451Arg
XM_006712245.3:c.1352A>G (COL4A3) XP_006712308.1:p.His451Arg
XM_011510556.2:c.113A>G (COL4A3) XP_011508858.1:p.His38Arg
XM_017003295.1:c.1352A>G (COL4A3) XP_016858784.1:p.His451Arg
XR_001738601.1:n.1490A>G (COL4A3)
XR_241280.3:n.1490A>G (COL4A3)
NM_000091.5:c.1352A>G (COL4A3) MANE Select NP_000082.2:p.His451Arg