Canonical Allele Identifier: CA501543674

Gene: ABCA5

Linked Data

• MyVariant Identifiers: chr17:g.67249787G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.69253646G>A , CM000679.2:g.69253646G>A	GRCh38
NC_000017.10:g.67249787G>A , CM000679.1:g.67249787G>A	GRCh37
NC_000017.9:g.64761382G>A	NCBI36
NG_034199.1:g.78537C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392676.8:c.4342C>T MANE Select	ENSP00000376443.2:p.Leu1448=
ENST00000392676.7:c.4342C>T	ENSP00000376443.2:p.Leu1448=
ENST00000586811.1:c.1240C>T	ENSP00000465351.1:p.Leu414=
ENST00000586995.5:c.3404C>T	ENSP00000467251.1:n.3404C>T
ENST00000588877.5:c.4342C>T	ENSP00000467882.1:p.Leu1448=
ENST00000591234.5:c.2284C>T	ENSP00000465766.1:n.2284C>T
NM_018672.4:c.4342C>T	NP_061142.2:p.Leu1448=
NM_172232.3:c.4342C>T	NP_758424.1:p.Leu1448=
NM_172232.4:c.4342C>T MANE Select	NP_758424.1:p.Leu1448=
NM_018672.5:c.4342C>T	NP_061142.2:p.Leu1448=