Canonical Allele Identifier: CA2639575367

Gene: ABCA5

Linked Data

• gnomAD v4: 17-69253709-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.69253709T>C , CM000679.2:g.69253709T>C	GRCh38
NC_000017.10:g.67249850T>C , CM000679.1:g.67249850T>C	GRCh37
NC_000017.9:g.64761445T>C	NCBI36
NG_034199.1:g.78474A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000392676.8:c.4321-42A>G MANE Select	ENSP00000376443.2:n.4321-42A>G
ENST00000392676.7:c.4321-42A>G	ENSP00000376443.2:n.4321-42A>G
ENST00000586811.1:c.1219-42A>G	ENSP00000465351.1:n.1219-42A>G
ENST00000586995.5:c.3383-42A>G	ENSP00000467251.1:n.3383-42A>G
ENST00000588877.5:c.4321-42A>G	ENSP00000467882.1:n.4321-42A>G
ENST00000591234.5:c.2263-42A>G	ENSP00000465766.1:n.2263-42A>G
NM_018672.4:c.4321-42A>G	NP_061142.2:n.4321-42A>G
NM_172232.3:c.4321-42A>G	NP_758424.1:n.4321-42A>G
NM_172232.4:c.4321-42A>G MANE Select	NP_758424.1:n.4321-42A>G
NM_018672.5:c.4321-42A>G	NP_061142.2:n.4321-42A>G