Canonical Allele Identifier: CA2272580206
Gene: ABCA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69253737T= , CM000679.2:g.69253737T= GRCh38
NC_000017.10:g.67249878T= , CM000679.1:g.67249878T= GRCh37
NC_000017.9:g.64761473T= NCBI36
NG_034199.1:g.78446A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392676.8:c.4320+57A= MANE Select ENSP00000376443.2:n.4320+57A=
ENST00000392676.7:c.4320+57A= ENSP00000376443.2:n.4320+57A=
ENST00000586811.1:c.1218+57A= ENSP00000465351.1:n.1218+57A=
ENST00000586995.5:c.3382+57A= ENSP00000467251.1:n.3382+57A=
ENST00000588877.5:c.4320+57A= ENSP00000467882.1:n.4320+57A=
ENST00000591234.5:c.2262+57A= ENSP00000465766.1:n.2262+57A=
NM_018672.4:c.4320+57A= NP_061142.2:n.4320+57A=
NM_172232.3:c.4320+57A= NP_758424.1:n.4320+57A=
NM_172232.4:c.4320+57A= MANE Select NP_758424.1:n.4320+57A=
NM_018672.5:c.4320+57A= NP_061142.2:n.4320+57A=