Canonical Allele Identifier: CA400824566

Gene: ABCA5

Linked Data

• dbSNP Id: rs1402163195
• gnomAD v2: 17-67249967-C-T
• gnomAD v4: 17-69253826-C-T
• MyVariant Identifiers: chr17:g.67249967C>T (hg19) ; chr17:g.69253826C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.69253826C>T , CM000679.2:g.69253826C>T	GRCh38
NC_000017.10:g.67249967C>T , CM000679.1:g.67249967C>T	GRCh37
NC_000017.9:g.64761562C>T	NCBI36
NG_034199.1:g.78357G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392676.8:c.4288G>A MANE Select	ENSP00000376443.2:p.Val1430Ile
ENST00000392676.7:c.4288G>A	ENSP00000376443.2:p.Val1430Ile
ENST00000586811.1:c.1186G>A	ENSP00000465351.1:p.Val396Ile
ENST00000586995.5:c.3350G>A	ENSP00000467251.1:n.3350G>A
ENST00000588877.5:c.4288G>A	ENSP00000467882.1:p.Val1430Ile
ENST00000591234.5:c.2230G>A	ENSP00000465766.1:n.2230G>A
NM_018672.4:c.4288G>A	NP_061142.2:p.Val1430Ile
NM_172232.3:c.4288G>A	NP_758424.1:p.Val1430Ile
NM_172232.4:c.4288G>A MANE Select	NP_758424.1:p.Val1430Ile
NM_018672.5:c.4288G>A	NP_061142.2:p.Val1430Ile