Canonical Allele Identifier: CA466504348

Gene: ABCA1

Linked Data

• MyVariant Identifiers: chr9:g.107568594C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.104806313C>T , CM000671.2:g.104806313C>T	GRCh38
NC_000009.11:g.107568594C>T , CM000671.1:g.107568594C>T	GRCh37
NC_000009.10:g.106608415C>T	NCBI36
NG_007981.1:g.126843G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374736.8:c.4392G>A MANE Select	ENSP00000363868.3:p.Gln1464=
ENST00000678995.1:c.4398G>A	ENSP00000504612.1:p.Gln1466=
ENST00000374736.7:c.4392G>A	ENSP00000363868.3:p.Gln1464=
NM_005502.3:c.4392G>A	NP_005493.2:p.Gln1464=
XM_005251773.1:c.4398G>A	XP_005251830.1:p.Gln1466=
XM_005251776.1:c.4218G>A	XP_005251833.1:p.Gln1406=
XM_011518339.1:c.4473G>A	XP_011516641.1:p.Gln1491=
XM_011518340.1:c.4473G>A	XP_011516642.1:p.Gln1491=
XM_011518341.1:c.4467G>A	XP_011516643.1:p.Gln1489=
XM_011518342.1:c.4035G>A	XP_011516644.1:p.Gln1345=
XM_011518343.1:c.4473G>A	XP_011516645.1:p.Gln1491=
XM_011518344.1:c.4473G>A	XP_011516646.1:p.Gln1491=
XM_005251773.3:c.4398G>A	XP_005251830.1:p.Gln1466=
XM_005251776.3:c.4218G>A	XP_005251833.1:p.Gln1406=
XM_011518339.3:c.4473G>A	XP_011516641.1:p.Gln1491=
XM_011518340.3:c.4473G>A	XP_011516642.1:p.Gln1491=
XM_011518341.3:c.4467G>A	XP_011516643.1:p.Gln1489=
XM_011518342.3:c.4035G>A	XP_011516644.1:p.Gln1345=
XM_011518344.2:c.4473G>A	XP_011516646.1:p.Gln1491=
XM_017014378.2:c.4473G>A	XP_016869867.1:p.Gln1491=
XM_017014379.2:c.4473G>A	XP_016869868.1:p.Gln1491=
XM_017014380.2:c.4473G>A	XP_016869869.1:p.Gln1491=
XM_017014381.2:c.4473G>A	XP_016869870.1:p.Gln1491=
XM_017014382.2:c.4335G>A	XP_016869871.1:p.Gln1445=
XR_001746223.1:n.4786G>A
NM_005502.4:c.4392G>A MANE Select	NP_005493.2:p.Gln1464=