Canonical Allele Identifier: CA2146627
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

ClinVar Variation Id: 551440
dbSNP Id: rs772958162

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227266455G>A , CM000664.2:g.227266455G>A GRCh38
NC_000002.11:g.228131171G>A , CM000664.1:g.228131171G>A GRCh37
NC_000002.10:g.227839415G>A NCBI36
NG_011591.1:g.106891G>A , LRG_230:g.106891G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000396578.8:c.1354G>A (COL4A3) MANE Select ENSP00000379823.3:p.Gly452Arg
ENST00000396578.7:c.1354G>A (COL4A3) ENSP00000379823.3:p.Gly452Arg
NM_000091.4:c.1354G>A , LRG_230t1:c.1354G>A (COL4A3) NP_000082.2:p.Gly452Arg
NR_102371.1:n.656-520C>T (MFF-DT)
XM_005246276.2:c.1354G>A (COL4A3) XP_005246333.1:p.Gly452Arg
XM_005246277.2:c.1354G>A (COL4A3) XP_005246334.1:p.Gly452Arg
XM_005246280.2:c.1354G>A (COL4A3) XP_005246337.1:p.Gly452Arg
XM_006712245.2:c.1354G>A (COL4A3) XP_006712308.1:p.Gly452Arg
XM_011510555.1:c.1354G>A (COL4A3) XP_011508857.1:p.Gly452Arg
XM_011510556.1:c.115G>A (COL4A3) XP_011508858.1:p.Gly39Arg
XR_241280.2:n.1492G>A (COL4A3)
XM_005246277.3:c.1354G>A (COL4A3) XP_005246334.1:p.Gly452Arg
XM_005246280.3:c.1354G>A (COL4A3) XP_005246337.1:p.Gly452Arg
XM_006712245.3:c.1354G>A (COL4A3) XP_006712308.1:p.Gly452Arg
XM_011510556.2:c.115G>A (COL4A3) XP_011508858.1:p.Gly39Arg
XM_017003295.1:c.1354G>A (COL4A3) XP_016858784.1:p.Gly452Arg
XR_001738601.1:n.1492G>A (COL4A3)
XR_241280.3:n.1492G>A (COL4A3)
NM_000091.5:c.1354G>A (COL4A3) MANE Select NP_000082.2:p.Gly452Arg