Canonical Allele Identifier: CA1143577641
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94030484G= , CM000663.2:g.94030484G= GRCh38
NC_000001.10:g.94496040G= , CM000663.1:g.94496040G= GRCh37
NC_000001.9:g.94268628G= NCBI36
NG_009073.1:g.95666C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4296C= MANE Select ENSP00000359245.3:p.Asp1432=
ENST00000370225.3:c.4296C= ENSP00000359245.3:p.Asp1432=
ENST00000536513.5:c.672C= ENSP00000439707.2:p.Asp224=
NM_000350.2:c.4296C= NP_000341.2:p.Asp1432=
NM_000350.3:c.4296C= MANE Select NP_000341.2:p.Asp1432=