Canonical Allele Identifier: CA374314147

Gene: ABCA1

Linked Data

• dbSNP Id: rs1382766437
• gnomAD v4: 9-104798529-G-T
• MyVariant Identifiers: chr9:g.107560810G>T (hg19) ; chr9:g.104798529G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.104798529G>T , CM000671.2:g.104798529G>T	GRCh38
NC_000009.11:g.107560810G>T , CM000671.1:g.107560810G>T	GRCh37
NC_000009.10:g.106600631G>T	NCBI36
NG_007981.1:g.134627C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374736.8:c.5013C>A MANE Select	ENSP00000363868.3:p.Ser1671Arg
ENST00000678995.1:c.5019C>A	ENSP00000504612.1:p.Ser1673Arg
ENST00000374736.7:c.5013C>A	ENSP00000363868.3:p.Ser1671Arg
NM_005502.3:c.5013C>A	NP_005493.2:p.Ser1671Arg
XM_005251773.1:c.5019C>A	XP_005251830.1:p.Ser1673Arg
XM_005251776.1:c.4839C>A	XP_005251833.1:p.Ser1613Arg
XM_011518339.1:c.5094C>A	XP_011516641.1:p.Ser1698Arg
XM_011518340.1:c.5094C>A	XP_011516642.1:p.Ser1698Arg
XM_011518341.1:c.5088C>A	XP_011516643.1:p.Ser1696Arg
XM_011518342.1:c.4656C>A	XP_011516644.1:p.Ser1552Arg
XM_011518343.1:c.5094C>A	XP_011516645.1:p.Ser1698Arg
XM_005251773.3:c.5019C>A	XP_005251830.1:p.Ser1673Arg
XM_005251776.3:c.4839C>A	XP_005251833.1:p.Ser1613Arg
XM_011518339.3:c.5094C>A	XP_011516641.1:p.Ser1698Arg
XM_011518340.3:c.5094C>A	XP_011516642.1:p.Ser1698Arg
XM_011518341.3:c.5088C>A	XP_011516643.1:p.Ser1696Arg
XM_011518342.3:c.4656C>A	XP_011516644.1:p.Ser1552Arg
XM_017014378.2:c.5094C>A	XP_016869867.1:p.Ser1698Arg
XM_017014379.2:c.5094C>A	XP_016869868.1:p.Ser1698Arg
XM_017014380.2:c.5094C>A	XP_016869869.1:p.Ser1698Arg
XM_017014381.2:c.5094C>A	XP_016869870.1:p.Ser1698Arg
XM_017014382.2:c.4956C>A	XP_016869871.1:p.Ser1652Arg
XR_001746223.1:n.5407C>A
NM_005502.4:c.5013C>A MANE Select	NP_005493.2:p.Ser1671Arg