Canonical Allele Identifier: CA476665993

Gene: ACAT1

Linked Data

• MyVariant Identifiers: chr11:g.108017997G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108147270G>T , CM000673.2:g.108147270G>T	GRCh38
NC_000011.9:g.108017997G>T , CM000673.1:g.108017997G>T	GRCh37
NC_000011.8:g.107523207G>T	NCBI36
NG_009888.1:g.30740G>T
NG_009888.2:g.35566G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265838.9:c.1164G>T MANE Select	ENSP00000265838.4:p.Gly388=
ENST00000671707.1:n.1259G>T
ENST00000672031.1:c.*151G>T	ENSP00000500463.1:n.*151G>T
ENST00000672284.1:c.894G>T	ENSP00000500444.1:p.Gly298=
ENST00000672354.1:c.1185G>T	ENSP00000500490.1:p.Arg395Ser
ENST00000672367.1:c.801G>T	ENSP00000500209.1:p.Gly267=
ENST00000672580.1:c.*419G>T	ENSP00000500366.1:n.*419G>T
ENST00000672907.1:c.849G>T	ENSP00000500928.1:p.Gly283=
ENST00000673000.1:n.1252G>T
ENST00000673531.1:c.894G>T	ENSP00000500163.1:p.Gly298=
ENST00000265838.8:c.1164G>T	ENSP00000265838.4:p.Gly388=
ENST00000533597.1:n.240G>T
NM_000019.3:c.1164G>T	NP_000010.1:p.Gly388=
XM_006718834.2:c.894G>T	XP_006718897.1:p.Gly298=
XM_006718835.2:c.894G>T	XP_006718898.1:p.Gly298=
XM_006718835.3:c.894G>T	XP_006718898.1:p.Gly298=
XM_017017681.1:c.894G>T	XP_016873170.1:p.Gly298=
XM_017017682.2:c.786G>T	XP_016873171.1:p.Gly262=
XM_017017683.2:c.786G>T	XP_016873172.1:p.Gly262=
XM_024448511.1:c.894G>T	XP_024304279.1:p.Gly298=
XM_024448512.1:c.894G>T	XP_024304280.1:p.Gly298=
XM_024448513.1:c.894G>T	XP_024304281.1:p.Gly298=
XM_024448514.1:c.894G>T	XP_024304282.1:p.Gly298=
XM_024448515.1:c.894G>T	XP_024304283.1:p.Gly298=
NM_000019.4:c.1164G>T MANE Select	NP_000010.1:p.Gly388=
NM_001386677.1:c.1185G>T	NP_001373606.1:p.Arg395Ser
NM_001386678.1:c.849G>T	NP_001373607.1:p.Gly283=
NM_001386679.1:c.867G>T	NP_001373608.1:p.Gly289=
NM_001386681.1:c.894G>T	NP_001373610.1:p.Gly298=
NM_001386682.1:c.894G>T	NP_001373611.1:p.Gly298=
NM_001386685.1:c.894G>T	NP_001373614.1:p.Gly298=
NM_001386686.1:c.894G>T	NP_001373615.1:p.Gly298=
NM_001386687.1:c.894G>T	NP_001373616.1:p.Gly298=
NM_001386688.1:c.894G>T	NP_001373617.1:p.Gly298=
NM_001386689.1:c.894G>T	NP_001373618.1:p.Gly298=
NM_001386690.1:c.894G>T	NP_001373619.1:p.Gly298=
NM_001386691.1:c.894G>T	NP_001373620.1:p.Gly298=
NR_170162.1:n.1139G>T
NR_170163.1:n.1197G>T