Canonical Allele Identifier: CA1181422641
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94047070G= , CM000663.2:g.94047070G= GRCh38
NC_000001.10:g.94512626G= , CM000663.1:g.94512626G= GRCh37
NC_000001.9:g.94285214G= NCBI36
NG_009073.1:g.79080C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2767C= MANE Select ENSP00000359245.3:p.Pro923=
ENST00000649773.1:c.2545C= ENSP00000496882.1:p.Pro849=
ENST00000370225.3:c.2767C= ENSP00000359245.3:p.Pro923=
ENST00000536513.5:c.-64-6981C= ENSP00000439707.2:n.-64-6981C=
NM_000350.2:c.2767C= NP_000341.2:p.Pro923=
NM_000350.3:c.2767C= MANE Select NP_000341.2:p.Pro923=