Canonical Allele Identifier: CA2663432063
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227312137A>C , CM000664.2:g.227312137A>C GRCh38
NC_000002.11:g.228176853A>C , CM000664.1:g.228176853A>C GRCh37
NC_000002.10:g.227885097A>C NCBI36
NG_011591.1:g.152573A>C , LRG_230:g.152573A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000471862.2:n.2538A>C (COL4A3)
ENST00000682257.1:n.502A>C (COL4A3)
ENST00000682970.1:n.578A>C (COL4A3)
ENST00000683077.1:n.2219A>C (COL4A3)
ENST00000684413.1:n.2847A>C (COL4A3)
ENST00000684724.1:n.701A>C (COL4A3)
ENST00000396578.8:c.*267A>C (COL4A3) MANE Select ENSP00000379823.3:n.*267A>C
ENST00000396578.7:c.*267A>C (COL4A3) ENSP00000379823.3:n.*267A>C
NM_000091.4:c.*267A>C , LRG_230t1:c.*267A>C (COL4A3) NP_000082.2:n.*267A>C
NR_102371.1:n.48-6482T>G (MFF-DT)
XM_005246276.2:c.*193A>C (COL4A3) XP_005246333.1:n.*193A>C
XM_005246277.2:c.*267A>C (COL4A3) XP_005246334.1:n.*267A>C
XM_011510556.1:c.*267A>C (COL4A3) XP_011508858.1:n.*267A>C
XR_241280.2:n.5240A>C (COL4A3)
XM_005246277.3:c.*267A>C (COL4A3) XP_005246334.1:n.*267A>C
XM_011510556.2:c.*267A>C (COL4A3) XP_011508858.1:n.*267A>C
XR_241280.3:n.5240A>C (COL4A3)
NM_000091.5:c.*267A>C (COL4A3) MANE Select NP_000082.2:n.*267A>C