Canonical Allele Identifier: CA1181398558
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94001895G= , CM000663.2:g.94001895G= GRCh38
NC_000001.10:g.94467451G= , CM000663.1:g.94467451G= GRCh37
NC_000001.9:g.94240039G= NCBI36
NG_009073.1:g.124255C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.6245C= MANE Select ENSP00000359245.3:p.Ala2082=
ENST00000370225.3:c.6245C= ENSP00000359245.3:p.Ala2082=
ENST00000465352.1:n.661C=
ENST00000536513.5:c.2621C= ENSP00000439707.2:p.Ala874=
NM_000350.2:c.6245C= NP_000341.2:p.Ala2082=
NM_000350.3:c.6245C= MANE Select NP_000341.2:p.Ala2082=