Canonical Allele Identifier: CA1998713834

Gene: ACAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108132328_108132329delinsCA , CM000673.2:g.108132328_108132329delinsCA	GRCh38
NC_000011.9:g.108003055_108003056delinsCA , CM000673.1:g.108003055_108003056delinsCA	GRCh37
NC_000011.8:g.107508265_107508266delinsCA	NCBI36
NG_009888.1:g.15798_15799delinsCA
NG_009888.2:g.20624_20625delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265838.9:c.120+374_120+375delinsCA MANE Select	ENSP00000265838.4:n.120+374_120+375delinsCA
ENST00000671707.1:n.215+374_215+375delinsCA
ENST00000672008.1:c.120+374_120+375delinsCA	ENSP00000500499.1:n.120+374_120+375delinsCA
ENST00000672031.1:c.120+374_120+375delinsCA	ENSP00000500463.1:n.120+374_120+375delinsCA
ENST00000672284.1:c.-151+374_-151+375delinsCA	ENSP00000500444.1:n.-151+374_-151+375delinsCA
ENST00000672354.1:c.120+374_120+375delinsCA	ENSP00000500490.1:n.120+374_120+375delinsCA
ENST00000672367.1:c.73-6570_73-6569delinsCA	ENSP00000500209.1:n.73-6570_73-6569delinsCA
ENST00000672580.1:c.120+374_120+375delinsCA	ENSP00000500366.1:n.120+374_120+375delinsCA
ENST00000672907.1:c.120+374_120+375delinsCA	ENSP00000500928.1:n.120+374_120+375delinsCA
ENST00000673000.1:n.208+374_208+375delinsCA
ENST00000673531.1:c.-151+374_-151+375delinsCA	ENSP00000500163.1:n.-151+374_-151+375delinsCA
ENST00000265838.8:c.120+374_120+375delinsCA	ENSP00000265838.4:n.120+374_120+375delinsCA
ENST00000299355.10:c.120+374_120+375delinsCA	ENSP00000299355.6:n.120+374_120+375delinsCA
ENST00000524833.5:n.160+374_160+375delinsCA
ENST00000527942.5:c.-151+374_-151+375delinsCA	ENSP00000433568.1:n.-151+374_-151+375delinsCA
ENST00000531813.5:c.120+374_120+375delinsCA	ENSP00000435965.1:n.120+374_120+375delinsCA
ENST00000531853.5:n.384+374_384+375delinsCA
NM_000019.3:c.120+374_120+375delinsCA	NP_000010.1:n.120+374_120+375delinsCA
XM_006718834.2:c.-151+374_-151+375delinsCA	XP_006718897.1:n.-151+374_-151+375delinsCA
XM_006718835.2:c.-151+374_-151+375delinsCA	XP_006718898.1:n.-151+374_-151+375delinsCA
XM_006718835.3:c.-151+374_-151+375delinsCA	XP_006718898.1:n.-151+374_-151+375delinsCA
XM_017017681.1:c.-151+374_-151+375delinsCA	XP_016873170.1:n.-151+374_-151+375delinsCA
XM_017017682.2:c.-158+374_-158+375delinsCA	XP_016873171.1:n.-158+374_-158+375delinsCA
XM_017017683.2:c.-158+374_-158+375delinsCA	XP_016873172.1:n.-158+374_-158+375delinsCA
XM_024448511.1:c.-151+374_-151+375delinsCA	XP_024304279.1:n.-151+374_-151+375delinsCA
XM_024448512.1:c.-151+374_-151+375delinsCA	XP_024304280.1:n.-151+374_-151+375delinsCA
XM_024448513.1:c.-151+374_-151+375delinsCA	XP_024304281.1:n.-151+374_-151+375delinsCA
XM_024448514.1:c.-151+374_-151+375delinsCA	XP_024304282.1:n.-151+374_-151+375delinsCA
XM_024448515.1:c.-151+374_-151+375delinsCA	XP_024304283.1:n.-151+374_-151+375delinsCA
NM_000019.4:c.120+374_120+375delinsCA MANE Select	NP_000010.1:n.120+374_120+375delinsCA
NM_001386677.1:c.120+374_120+375delinsCA	NP_001373606.1:n.120+374_120+375delinsCA
NM_001386678.1:c.120+374_120+375delinsCA	NP_001373607.1:n.120+374_120+375delinsCA
NM_001386679.1:c.-158+374_-158+375delinsCA	NP_001373608.1:n.-158+374_-158+375delinsCA
NM_001386681.1:c.-151+374_-151+375delinsCA	NP_001373610.1:n.-151+374_-151+375delinsCA
NM_001386682.1:c.-151+374_-151+375delinsCA	NP_001373611.1:n.-151+374_-151+375delinsCA
NM_001386685.1:c.-151+374_-151+375delinsCA	NP_001373614.1:n.-151+374_-151+375delinsCA
NM_001386686.1:c.-151+374_-151+375delinsCA	NP_001373615.1:n.-151+374_-151+375delinsCA
NM_001386687.1:c.-151+374_-151+375delinsCA	NP_001373616.1:n.-151+374_-151+375delinsCA
NM_001386688.1:c.-151+374_-151+375delinsCA	NP_001373617.1:n.-151+374_-151+375delinsCA
NM_001386689.1:c.-151+374_-151+375delinsCA	NP_001373618.1:n.-151+374_-151+375delinsCA
NM_001386690.1:c.-151+374_-151+375delinsCA	NP_001373619.1:n.-151+374_-151+375delinsCA
NM_001386691.1:c.-151+374_-151+375delinsCA	NP_001373620.1:n.-151+374_-151+375delinsCA
NR_170162.1:n.160+374_160+375delinsCA
NR_170163.1:n.254+374_254+375delinsCA