Canonical Allele Identifier: CA1181408100
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94011402G= , CM000663.2:g.94011402G= GRCh38
NC_000001.10:g.94476958G= , CM000663.1:g.94476958G= GRCh37
NC_000001.9:g.94249546G= NCBI36
NG_009073.1:g.114748C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.5461-17C= MANE Select ENSP00000359245.3:n.5461-17C=
ENST00000370225.3:c.5461-17C= ENSP00000359245.3:n.5461-17C=
ENST00000536513.5:c.1837-17C= ENSP00000439707.2:n.1837-17C=
NM_000350.2:c.5461-17C= NP_000341.2:n.5461-17C=
NM_000350.3:c.5461-17C= MANE Select NP_000341.2:n.5461-17C=