Canonical Allele Identifier: CA1332863177
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

dbSNP Id: rs994125899

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227312181T>G , CM000664.2:g.227312181T>G GRCh38
NC_000002.11:g.228176897T>G , CM000664.1:g.228176897T>G GRCh37
NC_000002.10:g.227885141T>G NCBI36
NG_011591.1:g.152617T>G , LRG_230:g.152617T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000471862.2:n.2582T>G (COL4A3)
ENST00000682257.1:n.546T>G (COL4A3)
ENST00000682970.1:n.622T>G (COL4A3)
ENST00000683077.1:n.2263T>G (COL4A3)
ENST00000684413.1:n.2891T>G (COL4A3)
ENST00000684724.1:n.745T>G (COL4A3)
ENST00000396578.8:c.*311T>G (COL4A3) MANE Select ENSP00000379823.3:n.*311T>G
ENST00000396578.7:c.*311T>G (COL4A3) ENSP00000379823.3:n.*311T>G
NM_000091.4:c.*311T>G , LRG_230t1:c.*311T>G (COL4A3) NP_000082.2:n.*311T>G
NR_102371.1:n.48-6526A>C (MFF-DT)
XM_005246276.2:c.*237T>G (COL4A3) XP_005246333.1:n.*237T>G
XM_005246277.2:c.*311T>G (COL4A3) XP_005246334.1:n.*311T>G
XM_011510556.1:c.*311T>G (COL4A3) XP_011508858.1:n.*311T>G
XR_241280.2:n.5284T>G (COL4A3)
XM_005246277.3:c.*311T>G (COL4A3) XP_005246334.1:n.*311T>G
XM_011510556.2:c.*311T>G (COL4A3) XP_011508858.1:n.*311T>G
XR_241280.3:n.5284T>G (COL4A3)
NM_000091.5:c.*311T>G (COL4A3) MANE Select NP_000082.2:n.*311T>G