Canonical Allele Identifier: CA1140725978
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021650T= , CM000663.2:g.94021650T= GRCh38
NC_000001.10:g.94487206T= , CM000663.1:g.94487206T= GRCh37
NC_000001.9:g.94259794T= NCBI36
NG_009073.1:g.104500A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4838A= MANE Select ENSP00000359245.3:p.Asp1613=
ENST00000370225.3:c.4838A= ENSP00000359245.3:p.Asp1613=
ENST00000460514.1:n.332A=
ENST00000536513.5:c.1214A= ENSP00000439707.2:p.Asp405=
NM_000350.2:c.4838A= NP_000341.2:p.Asp1613=
NM_000350.3:c.4838A= MANE Select NP_000341.2:p.Asp1613=