Canonical Allele Identifier: CA1181414560
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94029483C= , CM000663.2:g.94029483C= GRCh38
NC_000001.10:g.94495039C= , CM000663.1:g.94495039C= GRCh37
NC_000001.9:g.94267627C= NCBI36
NG_009073.1:g.96667G=

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.4501G= MANE Select ENSP00000359245.3:p.Glu1501=
ENST00000370225.3:c.4501G= ENSP00000359245.3:p.Glu1501=
ENST00000536513.5:c.877G= ENSP00000439707.2:p.Glu293=
NM_000350.2:c.4501G= NP_000341.2:p.Glu1501=
NM_000350.3:c.4501G= MANE Select NP_000341.2:p.Glu1501=