Canonical Allele Identifier: CA1998716925

Gene: ACAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108138708_108138711delinsCATT , CM000673.2:g.108138708_108138711delinsCATT	GRCh38
NC_000011.9:g.108009435_108009438delinsCATT , CM000673.1:g.108009435_108009438delinsCATT	GRCh37
NC_000011.8:g.107514645_107514648delinsCATT	NCBI36
NG_009888.1:g.22178_22181delinsCATT
NG_009888.2:g.27004_27007delinsCATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265838.9:c.436-190_436-187delinsCATT MANE Select	ENSP00000265838.4:n.436-190_436-187delinsCATT
ENST00000671707.1:n.531-190_531-187delinsCATT
ENST00000672008.1:c.315-190_315-187delinsCATT	ENSP00000500499.1:n.315-190_315-187delinsCATT
ENST00000672031.1:c.436-190_436-187delinsCATT	ENSP00000500463.1:n.436-190_436-187delinsCATT
ENST00000672284.1:c.166-190_166-187delinsCATT	ENSP00000500444.1:n.166-190_166-187delinsCATT
ENST00000672354.1:c.436-190_436-187delinsCATT	ENSP00000500490.1:n.436-190_436-187delinsCATT
ENST00000672367.1:c.73-190_73-187delinsCATT	ENSP00000500209.1:n.73-190_73-187delinsCATT
ENST00000672580.1:c.436-190_436-187delinsCATT	ENSP00000500366.1:n.436-190_436-187delinsCATT
ENST00000672907.1:c.121-190_121-187delinsCATT	ENSP00000500928.1:n.121-190_121-187delinsCATT
ENST00000673000.1:n.524-190_524-187delinsCATT
ENST00000673531.1:c.166-190_166-187delinsCATT	ENSP00000500163.1:n.166-190_166-187delinsCATT
ENST00000265838.8:c.436-190_436-187delinsCATT	ENSP00000265838.4:n.436-190_436-187delinsCATT
ENST00000528370.1:c.242-190_242-187delinsCATT
ENST00000531813.5:c.335-190_335-187delinsCATT	ENSP00000435965.1:n.335-190_335-187delinsCATT
NM_000019.3:c.436-190_436-187delinsCATT	NP_000010.1:n.436-190_436-187delinsCATT
XM_006718834.2:c.166-190_166-187delinsCATT	XP_006718897.1:n.166-190_166-187delinsCATT
XM_006718835.2:c.166-190_166-187delinsCATT	XP_006718898.1:n.166-190_166-187delinsCATT
XM_006718835.3:c.166-190_166-187delinsCATT	XP_006718898.1:n.166-190_166-187delinsCATT
XM_017017681.1:c.166-190_166-187delinsCATT	XP_016873170.1:n.166-190_166-187delinsCATT
XM_017017682.2:c.58-190_58-187delinsCATT	XP_016873171.1:n.58-190_58-187delinsCATT
XM_017017683.2:c.58-190_58-187delinsCATT	XP_016873172.1:n.58-190_58-187delinsCATT
XM_024448511.1:c.166-190_166-187delinsCATT	XP_024304279.1:n.166-190_166-187delinsCATT
XM_024448512.1:c.166-190_166-187delinsCATT	XP_024304280.1:n.166-190_166-187delinsCATT
XM_024448513.1:c.166-190_166-187delinsCATT	XP_024304281.1:n.166-190_166-187delinsCATT
XM_024448514.1:c.166-190_166-187delinsCATT	XP_024304282.1:n.166-190_166-187delinsCATT
XM_024448515.1:c.166-190_166-187delinsCATT	XP_024304283.1:n.166-190_166-187delinsCATT
NM_000019.4:c.436-190_436-187delinsCATT MANE Select	NP_000010.1:n.436-190_436-187delinsCATT
NM_001386677.1:c.436-190_436-187delinsCATT	NP_001373606.1:n.436-190_436-187delinsCATT
NM_001386678.1:c.121-190_121-187delinsCATT	NP_001373607.1:n.121-190_121-187delinsCATT
NM_001386679.1:c.139-190_139-187delinsCATT	NP_001373608.1:n.139-190_139-187delinsCATT
NM_001386681.1:c.166-190_166-187delinsCATT	NP_001373610.1:n.166-190_166-187delinsCATT
NM_001386682.1:c.166-190_166-187delinsCATT	NP_001373611.1:n.166-190_166-187delinsCATT
NM_001386685.1:c.166-190_166-187delinsCATT	NP_001373614.1:n.166-190_166-187delinsCATT
NM_001386686.1:c.166-190_166-187delinsCATT	NP_001373615.1:n.166-190_166-187delinsCATT
NM_001386687.1:c.166-190_166-187delinsCATT	NP_001373616.1:n.166-190_166-187delinsCATT
NM_001386688.1:c.166-190_166-187delinsCATT	NP_001373617.1:n.166-190_166-187delinsCATT
NM_001386689.1:c.166-190_166-187delinsCATT	NP_001373618.1:n.166-190_166-187delinsCATT
NM_001386690.1:c.166-190_166-187delinsCATT	NP_001373619.1:n.166-190_166-187delinsCATT
NM_001386691.1:c.166-190_166-187delinsCATT	NP_001373620.1:n.166-190_166-187delinsCATT
NR_170162.1:n.476-190_476-187delinsCATT
NR_170163.1:n.469-190_469-187delinsCATT