Canonical Allele Identifier: CA466510138

Gene: ABCA1

Linked Data

• MyVariant Identifiers: chr9:g.107591236A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.104828955A>G , CM000671.2:g.104828955A>G	GRCh38
NC_000009.11:g.107591236A>G , CM000671.1:g.107591236A>G	GRCh37
NC_000009.10:g.106631057A>G	NCBI36
NG_007981.1:g.104201T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000374736.8:c.2076T>C MANE Select	ENSP00000363868.3:p.Pro692=
ENST00000678995.1:c.2076T>C	ENSP00000504612.1:p.Pro692=
ENST00000374736.7:c.2076T>C	ENSP00000363868.3:p.Pro692=
ENST00000494467.1:n.249T>C
NM_005502.3:c.2076T>C	NP_005493.2:p.Pro692=
XM_005251773.1:c.2076T>C	XP_005251830.1:p.Pro692=
XM_005251776.1:c.1896T>C	XP_005251833.1:p.Pro632=
XM_011518339.1:c.2151T>C	XP_011516641.1:p.Pro717=
XM_011518340.1:c.2151T>C	XP_011516642.1:p.Pro717=
XM_011518341.1:c.2151T>C	XP_011516643.1:p.Pro717=
XM_011518342.1:c.1713T>C	XP_011516644.1:p.Pro571=
XM_011518343.1:c.2151T>C	XP_011516645.1:p.Pro717=
XM_011518344.1:c.2151T>C	XP_011516646.1:p.Pro717=
XM_005251773.3:c.2076T>C	XP_005251830.1:p.Pro692=
XM_005251776.3:c.1896T>C	XP_005251833.1:p.Pro632=
XM_011518339.3:c.2151T>C	XP_011516641.1:p.Pro717=
XM_011518340.3:c.2151T>C	XP_011516642.1:p.Pro717=
XM_011518341.3:c.2151T>C	XP_011516643.1:p.Pro717=
XM_011518342.3:c.1713T>C	XP_011516644.1:p.Pro571=
XM_011518344.2:c.2151T>C	XP_011516646.1:p.Pro717=
XM_017014378.2:c.2151T>C	XP_016869867.1:p.Pro717=
XM_017014379.2:c.2151T>C	XP_016869868.1:p.Pro717=
XM_017014380.2:c.2151T>C	XP_016869869.1:p.Pro717=
XM_017014381.2:c.2151T>C	XP_016869870.1:p.Pro717=
XM_017014382.2:c.2013T>C	XP_016869871.1:p.Pro671=
XR_001746223.1:n.2464T>C
NM_005502.4:c.2076T>C MANE Select	NP_005493.2:p.Pro692=