Canonical Allele Identifier: CA2663432114
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227312172T>A , CM000664.2:g.227312172T>A GRCh38
NC_000002.11:g.228176888T>A , CM000664.1:g.228176888T>A GRCh37
NC_000002.10:g.227885132T>A NCBI36
NG_011591.1:g.152608T>A , LRG_230:g.152608T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000471862.2:n.2573T>A (COL4A3)
ENST00000682257.1:n.537T>A (COL4A3)
ENST00000682970.1:n.613T>A (COL4A3)
ENST00000683077.1:n.2254T>A (COL4A3)
ENST00000684413.1:n.2882T>A (COL4A3)
ENST00000684724.1:n.736T>A (COL4A3)
ENST00000396578.8:c.*302T>A (COL4A3) MANE Select ENSP00000379823.3:n.*302T>A
ENST00000396578.7:c.*302T>A (COL4A3) ENSP00000379823.3:n.*302T>A
NM_000091.4:c.*302T>A , LRG_230t1:c.*302T>A (COL4A3) NP_000082.2:n.*302T>A
NR_102371.1:n.48-6517A>T (MFF-DT)
XM_005246276.2:c.*228T>A (COL4A3) XP_005246333.1:n.*228T>A
XM_005246277.2:c.*302T>A (COL4A3) XP_005246334.1:n.*302T>A
XM_011510556.1:c.*302T>A (COL4A3) XP_011508858.1:n.*302T>A
XR_241280.2:n.5275T>A (COL4A3)
XM_005246277.3:c.*302T>A (COL4A3) XP_005246334.1:n.*302T>A
XM_011510556.2:c.*302T>A (COL4A3) XP_011508858.1:n.*302T>A
XR_241280.3:n.5275T>A (COL4A3)
NM_000091.5:c.*302T>A (COL4A3) MANE Select NP_000082.2:n.*302T>A