Canonical Allele Identifier: CA431502665
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.228145688A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227280972A>C , CM000664.2:g.227280972A>C GRCh38
NC_000002.11:g.228145688A>C , CM000664.1:g.228145688A>C GRCh37
NC_000002.10:g.227853932A>C NCBI36
NG_011591.1:g.121408A>C , LRG_230:g.121408A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000396578.8:c.2454A>C (COL4A3) MANE Select ENSP00000379823.3:p.Gly818=
ENST00000396578.7:c.2454A>C (COL4A3) ENSP00000379823.3:p.Gly818=
NM_000091.4:c.2454A>C , LRG_230t1:c.2454A>C (COL4A3) NP_000082.2:p.Gly818=
NR_102371.1:n.329+732T>G (MFF-DT)
XM_005246276.2:c.2454A>C (COL4A3) XP_005246333.1:p.Gly818=
XM_005246277.2:c.2349A>C (COL4A3) XP_005246334.1:p.Gly783=
XM_005246280.2:c.2454A>C (COL4A3) XP_005246337.1:p.Gly818=
XM_006712245.2:c.2454A>C (COL4A3) XP_006712308.1:p.Gly818=
XM_011510555.1:c.2454A>C (COL4A3) XP_011508857.1:p.Gly818=
XM_011510556.1:c.1215A>C (COL4A3) XP_011508858.1:p.Gly405=
XR_241280.2:n.2592A>C (COL4A3)
XM_005246277.3:c.2349A>C (COL4A3) XP_005246334.1:p.Gly783=
XM_005246280.3:c.2454A>C (COL4A3) XP_005246337.1:p.Gly818=
XM_006712245.3:c.2454A>C (COL4A3) XP_006712308.1:p.Gly818=
XM_011510556.2:c.1215A>C (COL4A3) XP_011508858.1:p.Gly405=
XM_017003295.1:c.2454A>C (COL4A3) XP_016858784.1:p.Gly818=
XR_001738601.1:n.2592A>C (COL4A3)
XR_241280.3:n.2592A>C (COL4A3)
NM_000091.5:c.2454A>C (COL4A3) MANE Select NP_000082.2:p.Gly818=