Canonical Allele Identifier: CA431501974
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.228145272A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227280556A>G , CM000664.2:g.227280556A>G GRCh38
NC_000002.11:g.228145272A>G , CM000664.1:g.228145272A>G GRCh37
NC_000002.10:g.227853516A>G NCBI36
NG_011591.1:g.120992A>G , LRG_230:g.120992A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000396578.8:c.2340A>G (COL4A3) MANE Select ENSP00000379823.3:p.Gly780=
ENST00000396578.7:c.2340A>G (COL4A3) ENSP00000379823.3:p.Gly780=
NM_000091.4:c.2340A>G , LRG_230t1:c.2340A>G (COL4A3) NP_000082.2:p.Gly780=
NR_102371.1:n.330-981T>C (MFF-DT)
XM_005246276.2:c.2340A>G (COL4A3) XP_005246333.1:p.Gly780=
XM_005246277.2:c.2235A>G (COL4A3) XP_005246334.1:p.Gly745=
XM_005246280.2:c.2340A>G (COL4A3) XP_005246337.1:p.Gly780=
XM_006712245.2:c.2340A>G (COL4A3) XP_006712308.1:p.Gly780=
XM_011510555.1:c.2340A>G (COL4A3) XP_011508857.1:p.Gly780=
XM_011510556.1:c.1101A>G (COL4A3) XP_011508858.1:p.Gly367=
XR_241280.2:n.2478A>G (COL4A3)
XM_005246277.3:c.2235A>G (COL4A3) XP_005246334.1:p.Gly745=
XM_005246280.3:c.2340A>G (COL4A3) XP_005246337.1:p.Gly780=
XM_006712245.3:c.2340A>G (COL4A3) XP_006712308.1:p.Gly780=
XM_011510556.2:c.1101A>G (COL4A3) XP_011508858.1:p.Gly367=
XM_017003295.1:c.2340A>G (COL4A3) XP_016858784.1:p.Gly780=
XR_001738601.1:n.2478A>G (COL4A3)
XR_241280.3:n.2478A>G (COL4A3)
NM_000091.5:c.2340A>G (COL4A3) MANE Select NP_000082.2:p.Gly780=