Canonical Allele Identifier: CA2663432168
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227312198T>A , CM000664.2:g.227312198T>A GRCh38
NC_000002.11:g.228176914T>A , CM000664.1:g.228176914T>A GRCh37
NC_000002.10:g.227885158T>A NCBI36
NG_011591.1:g.152634T>A , LRG_230:g.152634T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000471862.2:n.2599T>A (COL4A3)
ENST00000682257.1:n.563T>A (COL4A3)
ENST00000682970.1:n.639T>A (COL4A3)
ENST00000683077.1:n.2280T>A (COL4A3)
ENST00000684413.1:n.2908T>A (COL4A3)
ENST00000684724.1:n.762T>A (COL4A3)
ENST00000396578.8:c.*328T>A (COL4A3) MANE Select ENSP00000379823.3:n.*328T>A
ENST00000396578.7:c.*328T>A (COL4A3) ENSP00000379823.3:n.*328T>A
NM_000091.4:c.*328T>A , LRG_230t1:c.*328T>A (COL4A3) NP_000082.2:n.*328T>A
NR_102371.1:n.48-6543A>T (MFF-DT)
XM_005246276.2:c.*254T>A (COL4A3) XP_005246333.1:n.*254T>A
XM_005246277.2:c.*328T>A (COL4A3) XP_005246334.1:n.*328T>A
XM_011510556.1:c.*328T>A (COL4A3) XP_011508858.1:n.*328T>A
XR_241280.2:n.5301T>A (COL4A3)
XM_005246277.3:c.*328T>A (COL4A3) XP_005246334.1:n.*328T>A
XM_011510556.2:c.*328T>A (COL4A3) XP_011508858.1:n.*328T>A
XR_241280.3:n.5301T>A (COL4A3)
NM_000091.5:c.*328T>A (COL4A3) MANE Select NP_000082.2:n.*328T>A