Canonical Allele Identifier: CA431509575
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.228176544A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227311828A>G , CM000664.2:g.227311828A>G GRCh38
NC_000002.11:g.228176544A>G , CM000664.1:g.228176544A>G GRCh37
NC_000002.10:g.227884788A>G NCBI36
NG_011591.1:g.152264A>G , LRG_230:g.152264A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000471862.2:n.2229A>G (COL4A3)
ENST00000682257.1:n.193A>G (COL4A3)
ENST00000682970.1:n.269A>G (COL4A3)
ENST00000683077.1:n.1910A>G (COL4A3)
ENST00000684413.1:n.2538A>G (COL4A3)
ENST00000684724.1:n.392A>G (COL4A3)
ENST00000396578.8:c.4971A>G (COL4A3) MANE Select ENSP00000379823.3:p.Lys1657=
ENST00000469504.2:c.764A>G (COL4A3) ENSP00000493493.1:n.764A>G
ENST00000643388.1:c.484A>G (COL4A3) ENSP00000495177.1:p.Asn162Asp
ENST00000396578.7:c.4971A>G (COL4A3) ENSP00000379823.3:p.Lys1657=
ENST00000469504.1:n.479A>G (COL4A3)
NM_000091.4:c.4971A>G , LRG_230t1:c.4971A>G (COL4A3) NP_000082.2:p.Lys1657=
NR_102371.1:n.48-6173T>C (MFF-DT)
XM_005246276.2:c.4798A>G (COL4A3) XP_005246333.1:p.Asn1600Asp
XM_005246277.2:c.4866A>G (COL4A3) XP_005246334.1:p.Lys1622=
XM_011510556.1:c.3732A>G (COL4A3) XP_011508858.1:p.Lys1244=
XR_241280.2:n.4931A>G (COL4A3)
XM_005246277.3:c.4866A>G (COL4A3) XP_005246334.1:p.Lys1622=
XM_011510556.2:c.3732A>G (COL4A3) XP_011508858.1:p.Lys1244=
XR_241280.3:n.4931A>G (COL4A3)
NM_000091.5:c.4971A>G (COL4A3) MANE Select NP_000082.2:p.Lys1657=