Canonical Allele Identifier: CA2663432088
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227312159T>A , CM000664.2:g.227312159T>A GRCh38
NC_000002.11:g.228176875T>A , CM000664.1:g.228176875T>A GRCh37
NC_000002.10:g.227885119T>A NCBI36
NG_011591.1:g.152595T>A , LRG_230:g.152595T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000471862.2:n.2560T>A (COL4A3)
ENST00000682257.1:n.524T>A (COL4A3)
ENST00000682970.1:n.600T>A (COL4A3)
ENST00000683077.1:n.2241T>A (COL4A3)
ENST00000684413.1:n.2869T>A (COL4A3)
ENST00000684724.1:n.723T>A (COL4A3)
ENST00000396578.8:c.*289T>A (COL4A3) MANE Select ENSP00000379823.3:n.*289T>A
ENST00000396578.7:c.*289T>A (COL4A3) ENSP00000379823.3:n.*289T>A
NM_000091.4:c.*289T>A , LRG_230t1:c.*289T>A (COL4A3) NP_000082.2:n.*289T>A
NR_102371.1:n.48-6504A>T (MFF-DT)
XM_005246276.2:c.*215T>A (COL4A3) XP_005246333.1:n.*215T>A
XM_005246277.2:c.*289T>A (COL4A3) XP_005246334.1:n.*289T>A
XM_011510556.1:c.*289T>A (COL4A3) XP_011508858.1:n.*289T>A
XR_241280.2:n.5262T>A (COL4A3)
XM_005246277.3:c.*289T>A (COL4A3) XP_005246334.1:n.*289T>A
XM_011510556.2:c.*289T>A (COL4A3) XP_011508858.1:n.*289T>A
XR_241280.3:n.5262T>A (COL4A3)
NM_000091.5:c.*289T>A (COL4A3) MANE Select NP_000082.2:n.*289T>A