Canonical Allele Identifier: CA2272580161
Gene: ABCA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69253657G= , CM000679.2:g.69253657G= GRCh38
NC_000017.10:g.67249798G= , CM000679.1:g.67249798G= GRCh37
NC_000017.9:g.64761393G= NCBI36
NG_034199.1:g.78526C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392676.8:c.4331C= MANE Select ENSP00000376443.2:p.Ala1444=
ENST00000392676.7:c.4331C= ENSP00000376443.2:p.Ala1444=
ENST00000586811.1:c.1229C= ENSP00000465351.1:p.Ala410=
ENST00000586995.5:c.3393C= ENSP00000467251.1:n.3393C=
ENST00000588877.5:c.4331C= ENSP00000467882.1:p.Ala1444=
ENST00000591234.5:c.2273C= ENSP00000465766.1:n.2273C=
NM_018672.4:c.4331C= NP_061142.2:p.Ala1444=
NM_172232.3:c.4331C= NP_758424.1:p.Ala1444=
NM_172232.4:c.4331C= MANE Select NP_758424.1:p.Ala1444=
NM_018672.5:c.4331C= NP_061142.2:p.Ala1444=