Canonical Allele Identifier: CA2793533746

Gene: ACAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108134422_108134423del , CM000673.2:g.108134422_108134423del	GRCh38
NC_000011.9:g.108005149_108005150del , CM000673.1:g.108005149_108005150del	GRCh37
NC_000011.8:g.107510359_107510360del	NCBI36
NG_009888.1:g.17892_17893del
NG_009888.2:g.22718_22719del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265838.9:c.334+106_334+107del MANE Select	ENSP00000265838.4:n.334+106_334+107del
ENST00000671707.1:n.429+106_429+107del
ENST00000672008.1:c.314+126_314+127del	ENSP00000500499.1:n.314+126_314+127del
ENST00000672031.1:c.334+106_334+107del	ENSP00000500463.1:n.334+106_334+107del
ENST00000672284.1:c.64+106_64+107del	ENSP00000500444.1:n.64+106_64+107del
ENST00000672354.1:c.334+106_334+107del	ENSP00000500490.1:n.334+106_334+107del
ENST00000672367.1:c.73-4476_73-4475del	ENSP00000500209.1:n.73-4476_73-4475del
ENST00000672580.1:c.334+106_334+107del	ENSP00000500366.1:n.334+106_334+107del
ENST00000672907.1:c.120+2468_120+2469del	ENSP00000500928.1:n.120+2468_120+2469del
ENST00000673000.1:n.422+106_422+107del
ENST00000673531.1:c.64+106_64+107del	ENSP00000500163.1:n.64+106_64+107del
ENST00000265838.8:c.334+106_334+107del	ENSP00000265838.4:n.334+106_334+107del
ENST00000299355.10:c.334+106_334+107del	ENSP00000299355.6:n.334+106_334+107del
ENST00000524833.5:n.480_481del
ENST00000527942.5:c.64+106_64+107del	ENSP00000433568.1:n.64+106_64+107del
ENST00000528370.1:c.140+106_140+107del
ENST00000531813.5:c.334+106_334+107del	ENSP00000435965.1:n.334+106_334+107del
NM_000019.3:c.334+106_334+107del	NP_000010.1:n.334+106_334+107del
XM_006718834.2:c.64+106_64+107del	XP_006718897.1:n.64+106_64+107del
XM_006718835.2:c.64+106_64+107del	XP_006718898.1:n.64+106_64+107del
XM_006718835.3:c.64+106_64+107del	XP_006718898.1:n.64+106_64+107del
XM_017017681.1:c.64+106_64+107del	XP_016873170.1:n.64+106_64+107del
XM_017017682.2:c.57+106_57+107del	XP_016873171.1:n.57+106_57+107del
XM_017017683.2:c.57+106_57+107del	XP_016873172.1:n.57+106_57+107del
XM_024448511.1:c.64+106_64+107del	XP_024304279.1:n.64+106_64+107del
XM_024448512.1:c.64+106_64+107del	XP_024304280.1:n.64+106_64+107del
XM_024448513.1:c.64+106_64+107del	XP_024304281.1:n.64+106_64+107del
XM_024448514.1:c.64+106_64+107del	XP_024304282.1:n.64+106_64+107del
XM_024448515.1:c.64+106_64+107del	XP_024304283.1:n.64+106_64+107del
NM_000019.4:c.334+106_334+107del MANE Select	NP_000010.1:n.334+106_334+107del
NM_001386677.1:c.334+106_334+107del	NP_001373606.1:n.334+106_334+107del
NM_001386678.1:c.120+2468_120+2469del	NP_001373607.1:n.120+2468_120+2469del
NM_001386679.1:c.37+126_37+127del	NP_001373608.1:n.37+126_37+127del
NM_001386681.1:c.64+106_64+107del	NP_001373610.1:n.64+106_64+107del
NM_001386682.1:c.64+106_64+107del	NP_001373611.1:n.64+106_64+107del
NM_001386685.1:c.64+106_64+107del	NP_001373614.1:n.64+106_64+107del
NM_001386686.1:c.64+106_64+107del	NP_001373615.1:n.64+106_64+107del
NM_001386687.1:c.64+106_64+107del	NP_001373616.1:n.64+106_64+107del
NM_001386688.1:c.64+106_64+107del	NP_001373617.1:n.64+106_64+107del
NM_001386689.1:c.64+106_64+107del	NP_001373618.1:n.64+106_64+107del
NM_001386690.1:c.64+106_64+107del	NP_001373619.1:n.64+106_64+107del
NM_001386691.1:c.64+106_64+107del	NP_001373620.1:n.64+106_64+107del
NR_170162.1:n.374+106_374+107del
NR_170163.1:n.468+106_468+107del