Canonical Allele Identifier: CA2663432090
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227312160G>T , CM000664.2:g.227312160G>T GRCh38
NC_000002.11:g.228176876G>T , CM000664.1:g.228176876G>T GRCh37
NC_000002.10:g.227885120G>T NCBI36
NG_011591.1:g.152596G>T , LRG_230:g.152596G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000471862.2:n.2561G>T (COL4A3)
ENST00000682257.1:n.525G>T (COL4A3)
ENST00000682970.1:n.601G>T (COL4A3)
ENST00000683077.1:n.2242G>T (COL4A3)
ENST00000684413.1:n.2870G>T (COL4A3)
ENST00000684724.1:n.724G>T (COL4A3)
ENST00000396578.8:c.*290G>T (COL4A3) MANE Select ENSP00000379823.3:n.*290G>T
ENST00000396578.7:c.*290G>T (COL4A3) ENSP00000379823.3:n.*290G>T
NM_000091.4:c.*290G>T , LRG_230t1:c.*290G>T (COL4A3) NP_000082.2:n.*290G>T
NR_102371.1:n.48-6505C>A (MFF-DT)
XM_005246276.2:c.*216G>T (COL4A3) XP_005246333.1:n.*216G>T
XM_005246277.2:c.*290G>T (COL4A3) XP_005246334.1:n.*290G>T
XM_011510556.1:c.*290G>T (COL4A3) XP_011508858.1:n.*290G>T
XR_241280.2:n.5263G>T (COL4A3)
XM_005246277.3:c.*290G>T (COL4A3) XP_005246334.1:n.*290G>T
XM_011510556.2:c.*290G>T (COL4A3) XP_011508858.1:n.*290G>T
XR_241280.3:n.5263G>T (COL4A3)
NM_000091.5:c.*290G>T (COL4A3) MANE Select NP_000082.2:n.*290G>T