Canonical Allele Identifier: CA1332863145
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

dbSNP Id: rs1574846484

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227312087G>A , CM000664.2:g.227312087G>A GRCh38
NC_000002.11:g.228176803G>A , CM000664.1:g.228176803G>A GRCh37
NC_000002.10:g.227885047G>A NCBI36
NG_011591.1:g.152523G>A , LRG_230:g.152523G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000471862.2:n.2488G>A (COL4A3)
ENST00000682257.1:n.452G>A (COL4A3)
ENST00000682970.1:n.528G>A (COL4A3)
ENST00000683077.1:n.2169G>A (COL4A3)
ENST00000684413.1:n.2797G>A (COL4A3)
ENST00000684724.1:n.651G>A (COL4A3)
ENST00000396578.8:c.*217G>A (COL4A3) MANE Select ENSP00000379823.3:n.*217G>A
ENST00000396578.7:c.*217G>A (COL4A3) ENSP00000379823.3:n.*217G>A
NM_000091.4:c.*217G>A , LRG_230t1:c.*217G>A (COL4A3) NP_000082.2:n.*217G>A
NR_102371.1:n.48-6432C>T (MFF-DT)
XM_005246276.2:c.*143G>A (COL4A3) XP_005246333.1:n.*143G>A
XM_005246277.2:c.*217G>A (COL4A3) XP_005246334.1:n.*217G>A
XM_011510556.1:c.*217G>A (COL4A3) XP_011508858.1:n.*217G>A
XR_241280.2:n.5190G>A (COL4A3)
XM_005246277.3:c.*217G>A (COL4A3) XP_005246334.1:n.*217G>A
XM_011510556.2:c.*217G>A (COL4A3) XP_011508858.1:n.*217G>A
XR_241280.3:n.5190G>A (COL4A3)
NM_000091.5:c.*217G>A (COL4A3) MANE Select NP_000082.2:n.*217G>A