Canonical Allele Identifier: CA1181422638
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94047058G= , CM000663.2:g.94047058G= GRCh38
NC_000001.10:g.94512614G= , CM000663.1:g.94512614G= GRCh37
NC_000001.9:g.94285202G= NCBI36
NG_009073.1:g.79092C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2779C= MANE Select ENSP00000359245.3:p.Pro927=
ENST00000649773.1:c.2557C= ENSP00000496882.1:p.Pro853=
ENST00000370225.3:c.2779C= ENSP00000359245.3:p.Pro927=
ENST00000536513.5:c.-64-6969C= ENSP00000439707.2:n.-64-6969C=
NM_000350.2:c.2779C= NP_000341.2:p.Pro927=
NM_000350.3:c.2779C= MANE Select NP_000341.2:p.Pro927=