Canonical Allele Identifier: CA1139894820
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94001891G= , CM000663.2:g.94001891G= GRCh38
NC_000001.10:g.94467447G= , CM000663.1:g.94467447G= GRCh37
NC_000001.9:g.94240035G= NCBI36
NG_009073.1:g.124259C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.6249C= MANE Select ENSP00000359245.3:p.Ile2083=
ENST00000370225.3:c.6249C= ENSP00000359245.3:p.Ile2083=
ENST00000465352.1:n.665C=
ENST00000536513.5:c.2625C= ENSP00000439707.2:p.Ile875=
NM_000350.2:c.6249C= NP_000341.2:p.Ile2083=
NM_000350.3:c.6249C= MANE Select NP_000341.2:p.Ile2083=