Canonical Allele Identifier: CA2272580189
Gene: ABCA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69253708T= , CM000679.2:g.69253708T= GRCh38
NC_000017.10:g.67249849T= , CM000679.1:g.67249849T= GRCh37
NC_000017.9:g.64761444T= NCBI36
NG_034199.1:g.78475A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392676.8:c.4321-41A= MANE Select ENSP00000376443.2:n.4321-41A=
ENST00000392676.7:c.4321-41A= ENSP00000376443.2:n.4321-41A=
ENST00000586811.1:c.1219-41A= ENSP00000465351.1:n.1219-41A=
ENST00000586995.5:c.3383-41A= ENSP00000467251.1:n.3383-41A=
ENST00000588877.5:c.4321-41A= ENSP00000467882.1:n.4321-41A=
ENST00000591234.5:c.2263-41A= ENSP00000465766.1:n.2263-41A=
NM_018672.4:c.4321-41A= NP_061142.2:n.4321-41A=
NM_172232.3:c.4321-41A= NP_758424.1:n.4321-41A=
NM_172232.4:c.4321-41A= MANE Select NP_758424.1:n.4321-41A=
NM_018672.5:c.4321-41A= NP_061142.2:n.4321-41A=