Canonical Allele Identifier: CA466510062

Gene: ABCA1

Linked Data

• MyVariant Identifiers: chr9:g.107591221A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.104828940A>G , CM000671.2:g.104828940A>G	GRCh38
NC_000009.11:g.107591221A>G , CM000671.1:g.107591221A>G	GRCh37
NC_000009.10:g.106631042A>G	NCBI36
NG_007981.1:g.104216T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374736.8:c.2091T>C MANE Select	ENSP00000363868.3:p.Ala697=
ENST00000678995.1:c.2091T>C	ENSP00000504612.1:p.Ala697=
ENST00000374736.7:c.2091T>C	ENSP00000363868.3:p.Ala697=
ENST00000494467.1:n.264T>C
NM_005502.3:c.2091T>C	NP_005493.2:p.Ala697=
XM_005251773.1:c.2091T>C	XP_005251830.1:p.Ala697=
XM_005251776.1:c.1911T>C	XP_005251833.1:p.Ala637=
XM_011518339.1:c.2166T>C	XP_011516641.1:p.Ala722=
XM_011518340.1:c.2166T>C	XP_011516642.1:p.Ala722=
XM_011518341.1:c.2166T>C	XP_011516643.1:p.Ala722=
XM_011518342.1:c.1728T>C	XP_011516644.1:p.Ala576=
XM_011518343.1:c.2166T>C	XP_011516645.1:p.Ala722=
XM_011518344.1:c.2166T>C	XP_011516646.1:p.Ala722=
XM_005251773.3:c.2091T>C	XP_005251830.1:p.Ala697=
XM_005251776.3:c.1911T>C	XP_005251833.1:p.Ala637=
XM_011518339.3:c.2166T>C	XP_011516641.1:p.Ala722=
XM_011518340.3:c.2166T>C	XP_011516642.1:p.Ala722=
XM_011518341.3:c.2166T>C	XP_011516643.1:p.Ala722=
XM_011518342.3:c.1728T>C	XP_011516644.1:p.Ala576=
XM_011518344.2:c.2166T>C	XP_011516646.1:p.Ala722=
XM_017014378.2:c.2166T>C	XP_016869867.1:p.Ala722=
XM_017014379.2:c.2166T>C	XP_016869868.1:p.Ala722=
XM_017014380.2:c.2166T>C	XP_016869869.1:p.Ala722=
XM_017014381.2:c.2166T>C	XP_016869870.1:p.Ala722=
XM_017014382.2:c.2028T>C	XP_016869871.1:p.Ala676=
XR_001746223.1:n.2479T>C
NM_005502.4:c.2091T>C MANE Select	NP_005493.2:p.Ala697=