Canonical Allele Identifier: CA1181408222
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021371G= , CM000663.2:g.94021371G= GRCh38
NC_000001.10:g.94486927G= , CM000663.1:g.94486927G= GRCh37
NC_000001.9:g.94259515G= NCBI36
NG_009073.1:g.104779C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4887C= MANE Select ENSP00000359245.3:p.Ser1629=
ENST00000370225.3:c.4887C= ENSP00000359245.3:p.Ser1629=
ENST00000460514.1:n.381C=
ENST00000536513.5:c.1263C= ENSP00000439707.2:p.Ser421=
NM_000350.2:c.4887C= NP_000341.2:p.Ser1629=
NM_000350.3:c.4887C= MANE Select NP_000341.2:p.Ser1629=