Canonical Allele Identifier: CA2663432086
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227312155A>T , CM000664.2:g.227312155A>T GRCh38
NC_000002.11:g.228176871A>T , CM000664.1:g.228176871A>T GRCh37
NC_000002.10:g.227885115A>T NCBI36
NG_011591.1:g.152591A>T , LRG_230:g.152591A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000471862.2:n.2556A>T (COL4A3)
ENST00000682257.1:n.520A>T (COL4A3)
ENST00000682970.1:n.596A>T (COL4A3)
ENST00000683077.1:n.2237A>T (COL4A3)
ENST00000684413.1:n.2865A>T (COL4A3)
ENST00000684724.1:n.719A>T (COL4A3)
ENST00000396578.8:c.*285A>T (COL4A3) MANE Select ENSP00000379823.3:n.*285A>T
ENST00000396578.7:c.*285A>T (COL4A3) ENSP00000379823.3:n.*285A>T
NM_000091.4:c.*285A>T , LRG_230t1:c.*285A>T (COL4A3) NP_000082.2:n.*285A>T
NR_102371.1:n.48-6500T>A (MFF-DT)
XM_005246276.2:c.*211A>T (COL4A3) XP_005246333.1:n.*211A>T
XM_005246277.2:c.*285A>T (COL4A3) XP_005246334.1:n.*285A>T
XM_011510556.1:c.*285A>T (COL4A3) XP_011508858.1:n.*285A>T
XR_241280.2:n.5258A>T (COL4A3)
XM_005246277.3:c.*285A>T (COL4A3) XP_005246334.1:n.*285A>T
XM_011510556.2:c.*285A>T (COL4A3) XP_011508858.1:n.*285A>T
XR_241280.3:n.5258A>T (COL4A3)
NM_000091.5:c.*285A>T (COL4A3) MANE Select NP_000082.2:n.*285A>T