Canonical Allele Identifier: CA5168161

Gene: ABCA1

Linked Data

• dbSNP Id: rs776100923
• ExAC: 9:107568598 C / T
• gnomAD v2: 9-107568598-C-T
• MyVariant Identifiers: chr9:g.107568598C>T (hg19) ; chr9:g.104806317C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.104806317C>T , CM000671.2:g.104806317C>T	GRCh38
NC_000009.11:g.107568598C>T , CM000671.1:g.107568598C>T	GRCh37
NC_000009.10:g.106608419C>T	NCBI36
NG_007981.1:g.126839G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374736.8:c.4388G>A MANE Select	ENSP00000363868.3:p.Cys1463Tyr
ENST00000678995.1:c.4394G>A	ENSP00000504612.1:p.Cys1465Tyr
ENST00000374736.7:c.4388G>A	ENSP00000363868.3:p.Cys1463Tyr
NM_005502.3:c.4388G>A	NP_005493.2:p.Cys1463Tyr
XM_005251773.1:c.4394G>A	XP_005251830.1:p.Cys1465Tyr
XM_005251776.1:c.4214G>A	XP_005251833.1:p.Cys1405Tyr
XM_011518339.1:c.4469G>A	XP_011516641.1:p.Cys1490Tyr
XM_011518340.1:c.4469G>A	XP_011516642.1:p.Cys1490Tyr
XM_011518341.1:c.4463G>A	XP_011516643.1:p.Cys1488Tyr
XM_011518342.1:c.4031G>A	XP_011516644.1:p.Cys1344Tyr
XM_011518343.1:c.4469G>A	XP_011516645.1:p.Cys1490Tyr
XM_011518344.1:c.4469G>A	XP_011516646.1:p.Cys1490Tyr
XM_005251773.3:c.4394G>A	XP_005251830.1:p.Cys1465Tyr
XM_005251776.3:c.4214G>A	XP_005251833.1:p.Cys1405Tyr
XM_011518339.3:c.4469G>A	XP_011516641.1:p.Cys1490Tyr
XM_011518340.3:c.4469G>A	XP_011516642.1:p.Cys1490Tyr
XM_011518341.3:c.4463G>A	XP_011516643.1:p.Cys1488Tyr
XM_011518342.3:c.4031G>A	XP_011516644.1:p.Cys1344Tyr
XM_011518344.2:c.4469G>A	XP_011516646.1:p.Cys1490Tyr
XM_017014378.2:c.4469G>A	XP_016869867.1:p.Cys1490Tyr
XM_017014379.2:c.4469G>A	XP_016869868.1:p.Cys1490Tyr
XM_017014380.2:c.4469G>A	XP_016869869.1:p.Cys1490Tyr
XM_017014381.2:c.4469G>A	XP_016869870.1:p.Cys1490Tyr
XM_017014382.2:c.4331G>A	XP_016869871.1:p.Cys1444Tyr
XR_001746223.1:n.4782G>A
NM_005502.4:c.4388G>A MANE Select	NP_005493.2:p.Cys1463Tyr