Canonical Allele Identifier: CA1143534161
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.93996119C= , CM000663.2:g.93996119C= GRCh38
NC_000001.10:g.94461675C= , CM000663.1:g.94461675C= GRCh37
NC_000001.9:g.94234263C= NCBI36
NG_009073.1:g.130031G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6806G= MANE Select ENSP00000359245.3:p.Arg2269=
ENST00000370225.3:c.6806G= ENSP00000359245.3:p.Arg2269=
ENST00000536513.5:c.3182G= ENSP00000439707.2:p.Arg1061=
NM_000350.2:c.6806G= NP_000341.2:p.Arg2269=
NM_000350.3:c.6806G= MANE Select NP_000341.2:p.Arg2269=