Canonical Allele Identifier: CA2555900956

Gene: ACAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108143699_108143700insGG , CM000673.2:g.108143699_108143700insGG	GRCh38
NC_000011.9:g.108014426_108014427insGG , CM000673.1:g.108014426_108014427insGG	GRCh37
NC_000011.8:g.107519636_107519637insGG	NCBI36
NG_009888.1:g.27169_27170insGG
NG_009888.2:g.31995_31996insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265838.9:c.941-284_941-283insGG MANE Select	ENSP00000265838.4:n.941-284_941-283insGG
ENST00000671707.1:n.1036-284_1036-283insGG
ENST00000672031.1:c.940+1149_940+1150insGG	ENSP00000500463.1:n.940+1149_940+1150insGG
ENST00000672284.1:c.671-284_671-283insGG	ENSP00000500444.1:n.671-284_671-283insGG
ENST00000672354.1:c.941-284_941-283insGG	ENSP00000500490.1:n.941-284_941-283insGG
ENST00000672367.1:c.578-284_578-283insGG	ENSP00000500209.1:n.578-284_578-283insGG
ENST00000672580.1:c.*196-284_*196-283insGG	ENSP00000500366.1:n.*196-284_*196-283insGG
ENST00000672907.1:c.626-284_626-283insGG	ENSP00000500928.1:n.626-284_626-283insGG
ENST00000673000.1:n.1029-284_1029-283insGG
ENST00000673531.1:c.671-284_671-283insGG	ENSP00000500163.1:n.671-284_671-283insGG
ENST00000265838.8:c.941-284_941-283insGG	ENSP00000265838.4:n.941-284_941-283insGG
ENST00000531813.5:c.*1562_*1563insGG	ENSP00000435965.1:n.*1562_*1563insGG
ENST00000532792.5:n.436-284_436-283insGG
ENST00000533610.1:n.402-284_402-283insGG
NM_000019.3:c.941-284_941-283insGG	NP_000010.1:n.941-284_941-283insGG
XM_006718834.2:c.671-284_671-283insGG	XP_006718897.1:n.671-284_671-283insGG
XM_006718835.2:c.671-284_671-283insGG	XP_006718898.1:n.671-284_671-283insGG
XM_006718835.3:c.671-284_671-283insGG	XP_006718898.1:n.671-284_671-283insGG
XM_017017681.1:c.671-284_671-283insGG	XP_016873170.1:n.671-284_671-283insGG
XM_017017682.2:c.563-284_563-283insGG	XP_016873171.1:n.563-284_563-283insGG
XM_017017683.2:c.563-284_563-283insGG	XP_016873172.1:n.563-284_563-283insGG
XM_024448511.1:c.671-284_671-283insGG	XP_024304279.1:n.671-284_671-283insGG
XM_024448512.1:c.671-284_671-283insGG	XP_024304280.1:n.671-284_671-283insGG
XM_024448513.1:c.671-284_671-283insGG	XP_024304281.1:n.671-284_671-283insGG
XM_024448514.1:c.671-284_671-283insGG	XP_024304282.1:n.671-284_671-283insGG
XM_024448515.1:c.671-284_671-283insGG	XP_024304283.1:n.671-284_671-283insGG
NM_000019.4:c.941-284_941-283insGG MANE Select	NP_000010.1:n.941-284_941-283insGG
NM_001386677.1:c.941-284_941-283insGG	NP_001373606.1:n.941-284_941-283insGG
NM_001386678.1:c.626-284_626-283insGG	NP_001373607.1:n.626-284_626-283insGG
NM_001386679.1:c.644-284_644-283insGG	NP_001373608.1:n.644-284_644-283insGG
NM_001386681.1:c.671-284_671-283insGG	NP_001373610.1:n.671-284_671-283insGG
NM_001386682.1:c.671-284_671-283insGG	NP_001373611.1:n.671-284_671-283insGG
NM_001386685.1:c.671-284_671-283insGG	NP_001373614.1:n.671-284_671-283insGG
NM_001386686.1:c.671-284_671-283insGG	NP_001373615.1:n.671-284_671-283insGG
NM_001386687.1:c.671-284_671-283insGG	NP_001373616.1:n.671-284_671-283insGG
NM_001386688.1:c.671-284_671-283insGG	NP_001373617.1:n.671-284_671-283insGG
NM_001386689.1:c.671-284_671-283insGG	NP_001373618.1:n.671-284_671-283insGG
NM_001386690.1:c.671-284_671-283insGG	NP_001373619.1:n.671-284_671-283insGG
NM_001386691.1:c.671-284_671-283insGG	NP_001373620.1:n.671-284_671-283insGG
NR_170162.1:n.980+1149_980+1150insGG
NR_170163.1:n.974-284_974-283insGG