Canonical Allele Identifier: CA2663431950
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227311971G>C , CM000664.2:g.227311971G>C GRCh38
NC_000002.11:g.228176687G>C , CM000664.1:g.228176687G>C GRCh37
NC_000002.10:g.227884931G>C NCBI36
NG_011591.1:g.152407G>C , LRG_230:g.152407G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000471862.2:n.2372G>C (COL4A3)
ENST00000682257.1:n.336G>C (COL4A3)
ENST00000682970.1:n.412G>C (COL4A3)
ENST00000683077.1:n.2053G>C (COL4A3)
ENST00000684413.1:n.2681G>C (COL4A3)
ENST00000684724.1:n.535G>C (COL4A3)
ENST00000396578.8:c.*101G>C (COL4A3) MANE Select ENSP00000379823.3:n.*101G>C
ENST00000396578.7:c.*101G>C (COL4A3) ENSP00000379823.3:n.*101G>C
NM_000091.4:c.*101G>C , LRG_230t1:c.*101G>C (COL4A3) NP_000082.2:n.*101G>C
NR_102371.1:n.48-6316C>G (MFF-DT)
XM_005246276.2:c.*27G>C (COL4A3) XP_005246333.1:n.*27G>C
XM_005246277.2:c.*101G>C (COL4A3) XP_005246334.1:n.*101G>C
XM_011510556.1:c.*101G>C (COL4A3) XP_011508858.1:n.*101G>C
XR_241280.2:n.5074G>C (COL4A3)
XM_005246277.3:c.*101G>C (COL4A3) XP_005246334.1:n.*101G>C
XM_011510556.2:c.*101G>C (COL4A3) XP_011508858.1:n.*101G>C
XR_241280.3:n.5074G>C (COL4A3)
NM_000091.5:c.*101G>C (COL4A3) MANE Select NP_000082.2:n.*101G>C