Canonical Allele Identifier: CA1998716875

Gene: ACAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108138630_108138632delinsCAA , CM000673.2:g.108138630_108138632delinsCAA	GRCh38
NC_000011.9:g.108009357_108009359delinsCAA , CM000673.1:g.108009357_108009359delinsCAA	GRCh37
NC_000011.8:g.107514567_107514569delinsCAA	NCBI36
NG_009888.1:g.22100_22102delinsCAA
NG_009888.2:g.26926_26928delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265838.9:c.436-268_436-266delinsCAA MANE Select	ENSP00000265838.4:n.436-268_436-266delinsCAA
ENST00000671707.1:n.531-268_531-266delinsCAA
ENST00000672008.1:c.315-268_315-266delinsCAA	ENSP00000500499.1:n.315-268_315-266delinsCAA
ENST00000672031.1:c.436-268_436-266delinsCAA	ENSP00000500463.1:n.436-268_436-266delinsCAA
ENST00000672284.1:c.166-268_166-266delinsCAA	ENSP00000500444.1:n.166-268_166-266delinsCAA
ENST00000672354.1:c.436-268_436-266delinsCAA	ENSP00000500490.1:n.436-268_436-266delinsCAA
ENST00000672367.1:c.73-268_73-266delinsCAA	ENSP00000500209.1:n.73-268_73-266delinsCAA
ENST00000672580.1:c.436-268_436-266delinsCAA	ENSP00000500366.1:n.436-268_436-266delinsCAA
ENST00000672907.1:c.121-268_121-266delinsCAA	ENSP00000500928.1:n.121-268_121-266delinsCAA
ENST00000673000.1:n.524-268_524-266delinsCAA
ENST00000673531.1:c.166-268_166-266delinsCAA	ENSP00000500163.1:n.166-268_166-266delinsCAA
ENST00000265838.8:c.436-268_436-266delinsCAA	ENSP00000265838.4:n.436-268_436-266delinsCAA
ENST00000528370.1:c.242-268_242-266delinsCAA
ENST00000531813.5:c.335-268_335-266delinsCAA	ENSP00000435965.1:n.335-268_335-266delinsCAA
NM_000019.3:c.436-268_436-266delinsCAA	NP_000010.1:n.436-268_436-266delinsCAA
XM_006718834.2:c.166-268_166-266delinsCAA	XP_006718897.1:n.166-268_166-266delinsCAA
XM_006718835.2:c.166-268_166-266delinsCAA	XP_006718898.1:n.166-268_166-266delinsCAA
XM_006718835.3:c.166-268_166-266delinsCAA	XP_006718898.1:n.166-268_166-266delinsCAA
XM_017017681.1:c.166-268_166-266delinsCAA	XP_016873170.1:n.166-268_166-266delinsCAA
XM_017017682.2:c.58-268_58-266delinsCAA	XP_016873171.1:n.58-268_58-266delinsCAA
XM_017017683.2:c.58-268_58-266delinsCAA	XP_016873172.1:n.58-268_58-266delinsCAA
XM_024448511.1:c.166-268_166-266delinsCAA	XP_024304279.1:n.166-268_166-266delinsCAA
XM_024448512.1:c.166-268_166-266delinsCAA	XP_024304280.1:n.166-268_166-266delinsCAA
XM_024448513.1:c.166-268_166-266delinsCAA	XP_024304281.1:n.166-268_166-266delinsCAA
XM_024448514.1:c.166-268_166-266delinsCAA	XP_024304282.1:n.166-268_166-266delinsCAA
XM_024448515.1:c.166-268_166-266delinsCAA	XP_024304283.1:n.166-268_166-266delinsCAA
NM_000019.4:c.436-268_436-266delinsCAA MANE Select	NP_000010.1:n.436-268_436-266delinsCAA
NM_001386677.1:c.436-268_436-266delinsCAA	NP_001373606.1:n.436-268_436-266delinsCAA
NM_001386678.1:c.121-268_121-266delinsCAA	NP_001373607.1:n.121-268_121-266delinsCAA
NM_001386679.1:c.139-268_139-266delinsCAA	NP_001373608.1:n.139-268_139-266delinsCAA
NM_001386681.1:c.166-268_166-266delinsCAA	NP_001373610.1:n.166-268_166-266delinsCAA
NM_001386682.1:c.166-268_166-266delinsCAA	NP_001373611.1:n.166-268_166-266delinsCAA
NM_001386685.1:c.166-268_166-266delinsCAA	NP_001373614.1:n.166-268_166-266delinsCAA
NM_001386686.1:c.166-268_166-266delinsCAA	NP_001373615.1:n.166-268_166-266delinsCAA
NM_001386687.1:c.166-268_166-266delinsCAA	NP_001373616.1:n.166-268_166-266delinsCAA
NM_001386688.1:c.166-268_166-266delinsCAA	NP_001373617.1:n.166-268_166-266delinsCAA
NM_001386689.1:c.166-268_166-266delinsCAA	NP_001373618.1:n.166-268_166-266delinsCAA
NM_001386690.1:c.166-268_166-266delinsCAA	NP_001373619.1:n.166-268_166-266delinsCAA
NM_001386691.1:c.166-268_166-266delinsCAA	NP_001373620.1:n.166-268_166-266delinsCAA
NR_170162.1:n.476-268_476-266delinsCAA
NR_170163.1:n.469-268_469-266delinsCAA