Canonical Allele Identifier: CA1998720400

Gene: ACAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108146146_108146149delinsCAGT , CM000673.2:g.108146146_108146149delinsCAGT	GRCh38
NC_000011.9:g.108016873_108016876delinsCAGT , CM000673.1:g.108016873_108016876delinsCAGT	GRCh37
NC_000011.8:g.107522083_107522086delinsCAGT	NCBI36
NG_009888.1:g.29616_29619delinsCAGT
NG_009888.2:g.34442_34445delinsCAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265838.9:c.1006-56_1006-53delinsCAGT MANE Select	ENSP00000265838.4:n.1006-56_1006-53delinsCAGT
ENST00000671707.1:n.1101-56_1101-53delinsCAGT
ENST00000672031.1:c.941-56_941-53delinsCAGT	ENSP00000500463.1:n.941-56_941-53delinsCAGT
ENST00000672284.1:c.736-56_736-53delinsCAGT	ENSP00000500444.1:n.736-56_736-53delinsCAGT
ENST00000672354.1:c.1006-56_1006-53delinsCAGT	ENSP00000500490.1:n.1006-56_1006-53delinsCAGT
ENST00000672367.1:c.643-56_643-53delinsCAGT	ENSP00000500209.1:n.643-56_643-53delinsCAGT
ENST00000672580.1:c.*261-56_*261-53delinsCAGT	ENSP00000500366.1:n.*261-56_*261-53delinsCAGT
ENST00000672907.1:c.691-56_691-53delinsCAGT	ENSP00000500928.1:n.691-56_691-53delinsCAGT
ENST00000673000.1:n.1094-56_1094-53delinsCAGT
ENST00000673531.1:c.736-56_736-53delinsCAGT	ENSP00000500163.1:n.736-56_736-53delinsCAGT
ENST00000265838.8:c.1006-56_1006-53delinsCAGT	ENSP00000265838.4:n.1006-56_1006-53delinsCAGT
ENST00000533597.1:n.26_29delinsCAGT
NM_000019.3:c.1006-56_1006-53delinsCAGT	NP_000010.1:n.1006-56_1006-53delinsCAGT
XM_006718834.2:c.736-56_736-53delinsCAGT	XP_006718897.1:n.736-56_736-53delinsCAGT
XM_006718835.2:c.736-56_736-53delinsCAGT	XP_006718898.1:n.736-56_736-53delinsCAGT
XM_006718835.3:c.736-56_736-53delinsCAGT	XP_006718898.1:n.736-56_736-53delinsCAGT
XM_017017681.1:c.736-56_736-53delinsCAGT	XP_016873170.1:n.736-56_736-53delinsCAGT
XM_017017682.2:c.628-56_628-53delinsCAGT	XP_016873171.1:n.628-56_628-53delinsCAGT
XM_017017683.2:c.628-56_628-53delinsCAGT	XP_016873172.1:n.628-56_628-53delinsCAGT
XM_024448511.1:c.736-56_736-53delinsCAGT	XP_024304279.1:n.736-56_736-53delinsCAGT
XM_024448512.1:c.736-56_736-53delinsCAGT	XP_024304280.1:n.736-56_736-53delinsCAGT
XM_024448513.1:c.736-56_736-53delinsCAGT	XP_024304281.1:n.736-56_736-53delinsCAGT
XM_024448514.1:c.736-56_736-53delinsCAGT	XP_024304282.1:n.736-56_736-53delinsCAGT
XM_024448515.1:c.736-56_736-53delinsCAGT	XP_024304283.1:n.736-56_736-53delinsCAGT
NM_000019.4:c.1006-56_1006-53delinsCAGT MANE Select	NP_000010.1:n.1006-56_1006-53delinsCAGT
NM_001386677.1:c.1006-56_1006-53delinsCAGT	NP_001373606.1:n.1006-56_1006-53delinsCAGT
NM_001386678.1:c.691-56_691-53delinsCAGT	NP_001373607.1:n.691-56_691-53delinsCAGT
NM_001386679.1:c.709-56_709-53delinsCAGT	NP_001373608.1:n.709-56_709-53delinsCAGT
NM_001386681.1:c.736-56_736-53delinsCAGT	NP_001373610.1:n.736-56_736-53delinsCAGT
NM_001386682.1:c.736-56_736-53delinsCAGT	NP_001373611.1:n.736-56_736-53delinsCAGT
NM_001386685.1:c.736-56_736-53delinsCAGT	NP_001373614.1:n.736-56_736-53delinsCAGT
NM_001386686.1:c.736-56_736-53delinsCAGT	NP_001373615.1:n.736-56_736-53delinsCAGT
NM_001386687.1:c.736-56_736-53delinsCAGT	NP_001373616.1:n.736-56_736-53delinsCAGT
NM_001386688.1:c.736-56_736-53delinsCAGT	NP_001373617.1:n.736-56_736-53delinsCAGT
NM_001386689.1:c.736-56_736-53delinsCAGT	NP_001373618.1:n.736-56_736-53delinsCAGT
NM_001386690.1:c.736-56_736-53delinsCAGT	NP_001373619.1:n.736-56_736-53delinsCAGT
NM_001386691.1:c.736-56_736-53delinsCAGT	NP_001373620.1:n.736-56_736-53delinsCAGT
NR_170162.1:n.981-56_981-53delinsCAGT
NR_170163.1:n.1039-56_1039-53delinsCAGT