Canonical Allele Identifier: CA1181426514
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94056768C= , CM000663.2:g.94056768C= GRCh38
NC_000001.10:g.94522324C= , CM000663.1:g.94522324C= GRCh37
NC_000001.9:g.94294912C= NCBI36
NG_009073.1:g.69382G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2215G= MANE Select ENSP00000359245.3:p.Ala739=
ENST00000649773.1:c.2161-1453G= ENSP00000496882.1:n.2161-1453G=
ENST00000370225.3:c.2215G= ENSP00000359245.3:p.Ala739=
ENST00000536513.5:c.-65+6406G= ENSP00000439707.2:n.-65+6406G=
NM_000350.2:c.2215G= NP_000341.2:p.Ala739=
NM_000350.3:c.2215G= MANE Select NP_000341.2:p.Ala739=