Canonical Allele Identifier: CA1181408113
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94011423A= , CM000663.2:g.94011423A= GRCh38
NC_000001.10:g.94476979A= , CM000663.1:g.94476979A= GRCh37
NC_000001.9:g.94249567A= NCBI36
NG_009073.1:g.114727T=

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.5461-38T= MANE Select ENSP00000359245.3:n.5461-38T=
ENST00000370225.3:c.5461-38T= ENSP00000359245.3:n.5461-38T=
ENST00000536513.5:c.1837-38T= ENSP00000439707.2:n.1837-38T=
NM_000350.2:c.5461-38T= NP_000341.2:n.5461-38T=
NM_000350.3:c.5461-38T= MANE Select NP_000341.2:n.5461-38T=