Canonical Allele Identifier: CA1141919367
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94029481C= , CM000663.2:g.94029481C= GRCh38
NC_000001.10:g.94495037C= , CM000663.1:g.94495037C= GRCh37
NC_000001.9:g.94267625C= NCBI36
NG_009073.1:g.96669G=

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.4503G= MANE Select ENSP00000359245.3:p.Glu1501=
ENST00000370225.3:c.4503G= ENSP00000359245.3:p.Glu1501=
ENST00000536513.5:c.879G= ENSP00000439707.2:p.Glu293=
NM_000350.2:c.4503G= NP_000341.2:p.Glu1501=
NM_000350.3:c.4503G= MANE Select NP_000341.2:p.Glu1501=