Canonical Allele Identifier: CA1869916633

Gene: ABCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.104826988G= , CM000671.2:g.104826988G=	GRCh38
NC_000009.11:g.107589269G= , CM000671.1:g.107589269G=	GRCh37
NC_000009.10:g.106629090G=	NCBI36
NG_007981.1:g.106168C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000374736.8:c.2297C= MANE Select	ENSP00000363868.3:p.Ala766=
ENST00000678995.1:c.2297C=	ENSP00000504612.1:p.Ala766=
ENST00000374736.7:c.2297C=	ENSP00000363868.3:p.Ala766=
ENST00000494467.1:n.470C=
NM_005502.3:c.2297C=	NP_005493.2:p.Ala766=
XM_005251773.1:c.2297C=	XP_005251830.1:p.Ala766=
XM_005251776.1:c.2117C=	XP_005251833.1:p.Ala706=
XM_011518339.1:c.2372C=	XP_011516641.1:p.Ala791=
XM_011518340.1:c.2372C=	XP_011516642.1:p.Ala791=
XM_011518341.1:c.2372C=	XP_011516643.1:p.Ala791=
XM_011518342.1:c.1934C=	XP_011516644.1:p.Ala645=
XM_011518343.1:c.2372C=	XP_011516645.1:p.Ala791=
XM_011518344.1:c.2372C=	XP_011516646.1:p.Ala791=
XM_005251773.3:c.2297C=	XP_005251830.1:p.Ala766=
XM_005251776.3:c.2117C=	XP_005251833.1:p.Ala706=
XM_011518339.3:c.2372C=	XP_011516641.1:p.Ala791=
XM_011518340.3:c.2372C=	XP_011516642.1:p.Ala791=
XM_011518341.3:c.2372C=	XP_011516643.1:p.Ala791=
XM_011518342.3:c.1934C=	XP_011516644.1:p.Ala645=
XM_011518344.2:c.2372C=	XP_011516646.1:p.Ala791=
XM_017014378.2:c.2372C=	XP_016869867.1:p.Ala791=
XM_017014379.2:c.2372C=	XP_016869868.1:p.Ala791=
XM_017014380.2:c.2372C=	XP_016869869.1:p.Ala791=
XM_017014381.2:c.2372C=	XP_016869870.1:p.Ala791=
XM_017014382.2:c.2234C=	XP_016869871.1:p.Ala745=
XR_001746223.1:n.2685C=
NM_005502.4:c.2297C= MANE Select	NP_005493.2:p.Ala766=