Canonical Allele Identifier: CA2663432009
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227312077G>C , CM000664.2:g.227312077G>C GRCh38
NC_000002.11:g.228176793G>C , CM000664.1:g.228176793G>C GRCh37
NC_000002.10:g.227885037G>C NCBI36
NG_011591.1:g.152513G>C , LRG_230:g.152513G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000471862.2:n.2478G>C (COL4A3)
ENST00000682257.1:n.442G>C (COL4A3)
ENST00000682970.1:n.518G>C (COL4A3)
ENST00000683077.1:n.2159G>C (COL4A3)
ENST00000684413.1:n.2787G>C (COL4A3)
ENST00000684724.1:n.641G>C (COL4A3)
ENST00000396578.8:c.*207G>C (COL4A3) MANE Select ENSP00000379823.3:n.*207G>C
ENST00000396578.7:c.*207G>C (COL4A3) ENSP00000379823.3:n.*207G>C
NM_000091.4:c.*207G>C , LRG_230t1:c.*207G>C (COL4A3) NP_000082.2:n.*207G>C
NR_102371.1:n.48-6422C>G (MFF-DT)
XM_005246276.2:c.*133G>C (COL4A3) XP_005246333.1:n.*133G>C
XM_005246277.2:c.*207G>C (COL4A3) XP_005246334.1:n.*207G>C
XM_011510556.1:c.*207G>C (COL4A3) XP_011508858.1:n.*207G>C
XR_241280.2:n.5180G>C (COL4A3)
XM_005246277.3:c.*207G>C (COL4A3) XP_005246334.1:n.*207G>C
XM_011510556.2:c.*207G>C (COL4A3) XP_011508858.1:n.*207G>C
XR_241280.3:n.5180G>C (COL4A3)
NM_000091.5:c.*207G>C (COL4A3) MANE Select NP_000082.2:n.*207G>C