Canonical Allele Identifier: CA1181398608
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94001920C= , CM000663.2:g.94001920C= GRCh38
NC_000001.10:g.94467476C= , CM000663.1:g.94467476C= GRCh37
NC_000001.9:g.94240064C= NCBI36
NG_009073.1:g.124230G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6220G= MANE Select ENSP00000359245.3:p.Gly2074=
ENST00000370225.3:c.6220G= ENSP00000359245.3:p.Gly2074=
ENST00000465352.1:n.636G=
ENST00000536513.5:c.2596G= ENSP00000439707.2:p.Gly866=
NM_000350.2:c.6220G= NP_000341.2:p.Gly2074=
NM_000350.3:c.6220G= MANE Select NP_000341.2:p.Gly2074=