Canonical Allele Identifier: CA476665530

Gene: ACAT1

Linked Data

• MyVariant Identifiers: chr11:g.108016979A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108146252A>T , CM000673.2:g.108146252A>T	GRCh38
NC_000011.9:g.108016979A>T , CM000673.1:g.108016979A>T	GRCh37
NC_000011.8:g.107522189A>T	NCBI36
NG_009888.1:g.29722A>T
NG_009888.2:g.34548A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265838.9:c.1056A>T MANE Select	ENSP00000265838.4:p.Val352=
ENST00000671707.1:n.1151A>T
ENST00000672031.1:c.*43A>T	ENSP00000500463.1:n.*43A>T
ENST00000672284.1:c.786A>T	ENSP00000500444.1:p.Val262=
ENST00000672354.1:c.1056A>T	ENSP00000500490.1:p.Val352=
ENST00000672367.1:c.693A>T	ENSP00000500209.1:p.Val231=
ENST00000672580.1:c.*311A>T	ENSP00000500366.1:n.*311A>T
ENST00000672907.1:c.741A>T	ENSP00000500928.1:p.Val247=
ENST00000673000.1:n.1144A>T
ENST00000673531.1:c.786A>T	ENSP00000500163.1:p.Val262=
ENST00000265838.8:c.1056A>T	ENSP00000265838.4:p.Val352=
ENST00000533597.1:n.132A>T
NM_000019.3:c.1056A>T	NP_000010.1:p.Val352=
XM_006718834.2:c.786A>T	XP_006718897.1:p.Val262=
XM_006718835.2:c.786A>T	XP_006718898.1:p.Val262=
XM_006718835.3:c.786A>T	XP_006718898.1:p.Val262=
XM_017017681.1:c.786A>T	XP_016873170.1:p.Val262=
XM_017017682.2:c.678A>T	XP_016873171.1:p.Val226=
XM_017017683.2:c.678A>T	XP_016873172.1:p.Val226=
XM_024448511.1:c.786A>T	XP_024304279.1:p.Val262=
XM_024448512.1:c.786A>T	XP_024304280.1:p.Val262=
XM_024448513.1:c.786A>T	XP_024304281.1:p.Val262=
XM_024448514.1:c.786A>T	XP_024304282.1:p.Val262=
XM_024448515.1:c.786A>T	XP_024304283.1:p.Val262=
NM_000019.4:c.1056A>T MANE Select	NP_000010.1:p.Val352=
NM_001386677.1:c.1056A>T	NP_001373606.1:p.Val352=
NM_001386678.1:c.741A>T	NP_001373607.1:p.Val247=
NM_001386679.1:c.759A>T	NP_001373608.1:p.Val253=
NM_001386681.1:c.786A>T	NP_001373610.1:p.Val262=
NM_001386682.1:c.786A>T	NP_001373611.1:p.Val262=
NM_001386685.1:c.786A>T	NP_001373614.1:p.Val262=
NM_001386686.1:c.786A>T	NP_001373615.1:p.Val262=
NM_001386687.1:c.786A>T	NP_001373616.1:p.Val262=
NM_001386688.1:c.786A>T	NP_001373617.1:p.Val262=
NM_001386689.1:c.786A>T	NP_001373618.1:p.Val262=
NM_001386690.1:c.786A>T	NP_001373619.1:p.Val262=
NM_001386691.1:c.786A>T	NP_001373620.1:p.Val262=
NR_170162.1:n.1031A>T
NR_170163.1:n.1089A>T