Canonical Allele Identifier: CA197399701

Gene: ABCA1

Linked Data

• dbSNP Id: rs1049624616
• gnomAD v3: 9-104915062-A-T
• gnomAD v4: 9-104915062-A-T
• MyVariant Identifiers: chr9:g.107677343A>T (hg19) ; chr9:g.104915062A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.104915062A>T , CM000671.2:g.104915062A>T	GRCh38
NC_000009.11:g.107677343A>T , CM000671.1:g.107677343A>T	GRCh37
NC_000009.10:g.106717164A>T	NCBI36
NG_007981.1:g.18094T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000374736.8:c.-92-11291T>A MANE Select	ENSP00000363868.3:n.-92-11291T>A
ENST00000678995.1:c.-92-11291T>A	ENSP00000504612.1:n.-92-11291T>A
ENST00000374733.1:c.-115+12873T>A	ENSP00000363865.1:n.-115+12873T>A
ENST00000374736.7:c.-92-11291T>A	ENSP00000363868.3:n.-92-11291T>A
ENST00000423487.6:c.-92-11291T>A	ENSP00000416623.2:n.-92-11291T>A
NM_005502.3:c.-92-11291T>A	NP_005493.2:n.-92-11291T>A
XM_005251773.1:c.-92-11291T>A	XP_005251830.1:n.-92-11291T>A
XM_005251776.1:c.-115+12873T>A	XP_005251833.1:n.-115+12873T>A
XM_011518339.1:c.-92-11291T>A	XP_011516641.1:n.-92-11291T>A
XM_011518341.1:c.-92-11291T>A	XP_011516643.1:n.-92-11291T>A
XM_011518342.1:c.-156+12873T>A	XP_011516644.1:n.-156+12873T>A
XM_011518343.1:c.-92-11291T>A	XP_011516645.1:n.-92-11291T>A
XM_011518344.1:c.-92-11291T>A	XP_011516646.1:n.-92-11291T>A
XR_428585.2:n.999-3600A>T
XR_428586.2:n.999-3600A>T
XR_428587.2:n.20+2722A>T
XM_005251773.3:c.-92-11291T>A	XP_005251830.1:n.-92-11291T>A
XM_005251776.3:c.-115+12873T>A	XP_005251833.1:n.-115+12873T>A
XM_011518339.3:c.-92-11291T>A	XP_011516641.1:n.-92-11291T>A
XM_011518341.3:c.-92-11291T>A	XP_011516643.1:n.-92-11291T>A
XM_011518342.3:c.-156+12873T>A	XP_011516644.1:n.-156+12873T>A
XM_011518344.2:c.-92-11291T>A	XP_011516646.1:n.-92-11291T>A
XR_001746223.1:n.222-11291T>A
NM_005502.4:c.-92-11291T>A MANE Select	NP_005493.2:n.-92-11291T>A