Canonical Allele Identifier: CA10626132

Gene: ABCA1

Linked Data

• ClinVar Variation Id: 364353
• ClinVar RCV Id: RCV000297873 ; RCV000361968
• dbSNP Id: rs202165873
• gnomAD v2: 9-107545269-C-T
• gnomAD v3: 9-104782988-C-T
• gnomAD v4: 9-104782988-C-T
• MyVariant Identifiers: chr9:g.107545269C>T (hg19) ; chr9:g.104782988C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.104782988C>T , CM000671.2:g.104782988C>T	GRCh38
NC_000009.11:g.107545269C>T , CM000671.1:g.107545269C>T	GRCh37
NC_000009.10:g.106585090C>T	NCBI36
NG_007981.1:g.150168G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374736.8:c.*1327G>A MANE Select	ENSP00000363868.3:n.*1327G>A
ENST00000678995.1:c.*1327G>A	ENSP00000504612.1:n.*1327G>A
ENST00000374736.7:c.*1327G>A	ENSP00000363868.3:n.*1327G>A
NM_005502.3:c.*1327G>A	NP_005493.2:n.*1327G>A
XM_005251773.1:c.*1327G>A	XP_005251830.1:n.*1327G>A
XM_005251776.1:c.*1327G>A	XP_005251833.1:n.*1327G>A
XM_011518339.1:c.*1327G>A	XP_011516641.1:n.*1327G>A
XM_011518340.1:c.*1327G>A	XP_011516642.1:n.*1327G>A
XM_011518341.1:c.*1327G>A	XP_011516643.1:n.*1327G>A
XM_011518342.1:c.*1327G>A	XP_011516644.1:n.*1327G>A
XM_005251773.3:c.*1327G>A	XP_005251830.1:n.*1327G>A
XM_005251776.3:c.*1327G>A	XP_005251833.1:n.*1327G>A
XM_011518339.3:c.*1327G>A	XP_011516641.1:n.*1327G>A
XM_011518340.3:c.*1327G>A	XP_011516642.1:n.*1327G>A
XM_011518341.3:c.*1327G>A	XP_011516643.1:n.*1327G>A
XM_011518342.3:c.*1327G>A	XP_011516644.1:n.*1327G>A
XM_017014378.2:c.*1327G>A	XP_016869867.1:n.*1327G>A
XM_017014379.2:c.*1327G>A	XP_016869868.1:n.*1327G>A
XM_017014380.2:c.*1327G>A	XP_016869869.1:n.*1327G>A
XM_017014381.2:c.*1327G>A	XP_016869870.1:n.*1327G>A
XM_017014382.2:c.*1327G>A	XP_016869871.1:n.*1327G>A
NM_005502.4:c.*1327G>A MANE Select	NP_005493.2:n.*1327G>A