Canonical Allele Identifier: CA400824319

Gene: ABCA5

Linked Data

• MyVariant Identifiers: chr17:g.67249801A>G (hg19) ; chr17:g.69253660A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.69253660A>G , CM000679.2:g.69253660A>G	GRCh38
NC_000017.10:g.67249801A>G , CM000679.1:g.67249801A>G	GRCh37
NC_000017.9:g.64761396A>G	NCBI36
NG_034199.1:g.78523T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392676.8:c.4328T>C MANE Select	ENSP00000376443.2:p.Phe1443Ser
ENST00000392676.7:c.4328T>C	ENSP00000376443.2:p.Phe1443Ser
ENST00000586811.1:c.1226T>C	ENSP00000465351.1:p.Phe409Ser
ENST00000586995.5:c.3390T>C	ENSP00000467251.1:n.3390T>C
ENST00000588877.5:c.4328T>C	ENSP00000467882.1:p.Phe1443Ser
ENST00000591234.5:c.2270T>C	ENSP00000465766.1:n.2270T>C
NM_018672.4:c.4328T>C	NP_061142.2:p.Phe1443Ser
NM_172232.3:c.4328T>C	NP_758424.1:p.Phe1443Ser
NM_172232.4:c.4328T>C MANE Select	NP_758424.1:p.Phe1443Ser
NM_018672.5:c.4328T>C	NP_061142.2:p.Phe1443Ser