Canonical Allele Identifier: CA1181408566
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021673G= , CM000663.2:g.94021673G= GRCh38
NC_000001.10:g.94487229G= , CM000663.1:g.94487229G= GRCh37
NC_000001.9:g.94259817G= NCBI36
NG_009073.1:g.104477C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4815C= MANE Select ENSP00000359245.3:p.Phe1605=
ENST00000370225.3:c.4815C= ENSP00000359245.3:p.Phe1605=
ENST00000460514.1:n.309C=
ENST00000536513.5:c.1191C= ENSP00000439707.2:p.Phe397=
NM_000350.2:c.4815C= NP_000341.2:p.Phe1605=
NM_000350.3:c.4815C= MANE Select NP_000341.2:p.Phe1605=