Canonical Allele Identifier: CA2503169332

Gene: ACAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108134515_108134516insCTG , CM000673.2:g.108134515_108134516insCTG	GRCh38
NC_000011.9:g.108005242_108005243insCTG , CM000673.1:g.108005242_108005243insCTG	GRCh37
NC_000011.8:g.107510452_107510453insCTG	NCBI36
NG_009888.1:g.17985_17986insCTG
NG_009888.2:g.22811_22812insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265838.9:c.334+199_334+200insCTG MANE Select	ENSP00000265838.4:n.334+199_334+200insCTG
ENST00000671707.1:n.429+199_429+200insCTG
ENST00000672008.1:c.314+219_314+220insCTG	ENSP00000500499.1:n.314+219_314+220insCTG
ENST00000672031.1:c.334+199_334+200insCTG	ENSP00000500463.1:n.334+199_334+200insCTG
ENST00000672284.1:c.64+199_64+200insCTG	ENSP00000500444.1:n.64+199_64+200insCTG
ENST00000672354.1:c.334+199_334+200insCTG	ENSP00000500490.1:n.334+199_334+200insCTG
ENST00000672367.1:c.73-4383_73-4382insCTG	ENSP00000500209.1:n.73-4383_73-4382insCTG
ENST00000672580.1:c.334+199_334+200insCTG	ENSP00000500366.1:n.334+199_334+200insCTG
ENST00000672907.1:c.120+2561_120+2562insCTG	ENSP00000500928.1:n.120+2561_120+2562insCTG
ENST00000673000.1:n.422+199_422+200insCTG
ENST00000673531.1:c.64+199_64+200insCTG	ENSP00000500163.1:n.64+199_64+200insCTG
ENST00000265838.8:c.334+199_334+200insCTG	ENSP00000265838.4:n.334+199_334+200insCTG
ENST00000299355.10:c.334+199_334+200insCTG	ENSP00000299355.6:n.334+199_334+200insCTG
ENST00000527942.5:c.64+199_64+200insCTG	ENSP00000433568.1:n.64+199_64+200insCTG
ENST00000528370.1:c.140+199_140+200insCTG
ENST00000531813.5:c.334+199_334+200insCTG	ENSP00000435965.1:n.334+199_334+200insCTG
NM_000019.3:c.334+199_334+200insCTG	NP_000010.1:n.334+199_334+200insCTG
XM_006718834.2:c.64+199_64+200insCTG	XP_006718897.1:n.64+199_64+200insCTG
XM_006718835.2:c.64+199_64+200insCTG	XP_006718898.1:n.64+199_64+200insCTG
XM_006718835.3:c.64+199_64+200insCTG	XP_006718898.1:n.64+199_64+200insCTG
XM_017017681.1:c.64+199_64+200insCTG	XP_016873170.1:n.64+199_64+200insCTG
XM_017017682.2:c.57+199_57+200insCTG	XP_016873171.1:n.57+199_57+200insCTG
XM_017017683.2:c.57+199_57+200insCTG	XP_016873172.1:n.57+199_57+200insCTG
XM_024448511.1:c.64+199_64+200insCTG	XP_024304279.1:n.64+199_64+200insCTG
XM_024448512.1:c.64+199_64+200insCTG	XP_024304280.1:n.64+199_64+200insCTG
XM_024448513.1:c.64+199_64+200insCTG	XP_024304281.1:n.64+199_64+200insCTG
XM_024448514.1:c.64+199_64+200insCTG	XP_024304282.1:n.64+199_64+200insCTG
XM_024448515.1:c.64+199_64+200insCTG	XP_024304283.1:n.64+199_64+200insCTG
NM_000019.4:c.334+199_334+200insCTG MANE Select	NP_000010.1:n.334+199_334+200insCTG
NM_001386677.1:c.334+199_334+200insCTG	NP_001373606.1:n.334+199_334+200insCTG
NM_001386678.1:c.120+2561_120+2562insCTG	NP_001373607.1:n.120+2561_120+2562insCTG
NM_001386679.1:c.37+219_37+220insCTG	NP_001373608.1:n.37+219_37+220insCTG
NM_001386681.1:c.64+199_64+200insCTG	NP_001373610.1:n.64+199_64+200insCTG
NM_001386682.1:c.64+199_64+200insCTG	NP_001373611.1:n.64+199_64+200insCTG
NM_001386685.1:c.64+199_64+200insCTG	NP_001373614.1:n.64+199_64+200insCTG
NM_001386686.1:c.64+199_64+200insCTG	NP_001373615.1:n.64+199_64+200insCTG
NM_001386687.1:c.64+199_64+200insCTG	NP_001373616.1:n.64+199_64+200insCTG
NM_001386688.1:c.64+199_64+200insCTG	NP_001373617.1:n.64+199_64+200insCTG
NM_001386689.1:c.64+199_64+200insCTG	NP_001373618.1:n.64+199_64+200insCTG
NM_001386690.1:c.64+199_64+200insCTG	NP_001373619.1:n.64+199_64+200insCTG
NM_001386691.1:c.64+199_64+200insCTG	NP_001373620.1:n.64+199_64+200insCTG
NR_170162.1:n.374+199_374+200insCTG
NR_170163.1:n.468+199_468+200insCTG