Canonical Allele Identifier: CA1181408000
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94011315C= , CM000663.2:g.94011315C= GRCh38
NC_000001.10:g.94476871C= , CM000663.1:g.94476871C= GRCh37
NC_000001.9:g.94249459C= NCBI36
NG_009073.1:g.114835G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.5531G= MANE Select ENSP00000359245.3:p.Gly1844=
ENST00000370225.3:c.5531G= ENSP00000359245.3:p.Gly1844=
ENST00000536513.5:c.1907G= ENSP00000439707.2:p.Gly636=
NM_000350.2:c.5531G= NP_000341.2:p.Gly1844=
NM_000350.3:c.5531G= MANE Select NP_000341.2:p.Gly1844=