Canonical Allele Identifier: CA2615813483

Gene: ACAT1

Linked Data

• gnomAD v4: 11-108135336-ATTCTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108135338_108135342del , CM000673.2:g.108135338_108135342del	GRCh38
NC_000011.9:g.108006065_108006069del , CM000673.1:g.108006065_108006069del	GRCh37
NC_000011.8:g.107511275_107511279del	NCBI36
NG_009888.1:g.18808_18812del
NG_009888.2:g.23634_23638del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265838.9:c.435+96_435+100del MANE Select	ENSP00000265838.4:n.435+96_435+100del
ENST00000671707.1:n.530+96_530+100del
ENST00000672008.1:c.314+1042_314+1046del	ENSP00000500499.1:n.314+1042_314+1046del
ENST00000672031.1:c.435+96_435+100del	ENSP00000500463.1:n.435+96_435+100del
ENST00000672284.1:c.165+96_165+100del	ENSP00000500444.1:n.165+96_165+100del
ENST00000672354.1:c.435+96_435+100del	ENSP00000500490.1:n.435+96_435+100del
ENST00000672367.1:c.73-3560_73-3556del	ENSP00000500209.1:n.73-3560_73-3556del
ENST00000672580.1:c.435+96_435+100del	ENSP00000500366.1:n.435+96_435+100del
ENST00000672907.1:c.120+3384_120+3388del	ENSP00000500928.1:n.120+3384_120+3388del
ENST00000673000.1:n.523+96_523+100del
ENST00000673531.1:c.165+96_165+100del	ENSP00000500163.1:n.165+96_165+100del
ENST00000265838.8:c.435+96_435+100del	ENSP00000265838.4:n.435+96_435+100del
ENST00000299355.10:c.435+96_435+100del	ENSP00000299355.6:n.435+96_435+100del
ENST00000528370.1:c.241+96_241+100del
ENST00000531813.5:c.334+1022_334+1026del	ENSP00000435965.1:n.334+1022_334+1026del
NM_000019.3:c.435+96_435+100del	NP_000010.1:n.435+96_435+100del
XM_006718834.2:c.165+96_165+100del	XP_006718897.1:n.165+96_165+100del
XM_006718835.2:c.165+96_165+100del	XP_006718898.1:n.165+96_165+100del
XM_006718835.3:c.165+96_165+100del	XP_006718898.1:n.165+96_165+100del
XM_017017681.1:c.165+96_165+100del	XP_016873170.1:n.165+96_165+100del
XM_017017682.2:c.57+1022_57+1026del	XP_016873171.1:n.57+1022_57+1026del
XM_017017683.2:c.57+1022_57+1026del	XP_016873172.1:n.57+1022_57+1026del
XM_024448511.1:c.165+96_165+100del	XP_024304279.1:n.165+96_165+100del
XM_024448512.1:c.165+96_165+100del	XP_024304280.1:n.165+96_165+100del
XM_024448513.1:c.165+96_165+100del	XP_024304281.1:n.165+96_165+100del
XM_024448514.1:c.165+96_165+100del	XP_024304282.1:n.165+96_165+100del
XM_024448515.1:c.165+96_165+100del	XP_024304283.1:n.165+96_165+100del
NM_000019.4:c.435+96_435+100del MANE Select	NP_000010.1:n.435+96_435+100del
NM_001386677.1:c.435+96_435+100del	NP_001373606.1:n.435+96_435+100del
NM_001386678.1:c.120+3384_120+3388del	NP_001373607.1:n.120+3384_120+3388del
NM_001386679.1:c.138+96_138+100del	NP_001373608.1:n.138+96_138+100del
NM_001386681.1:c.165+96_165+100del	NP_001373610.1:n.165+96_165+100del
NM_001386682.1:c.165+96_165+100del	NP_001373611.1:n.165+96_165+100del
NM_001386685.1:c.165+96_165+100del	NP_001373614.1:n.165+96_165+100del
NM_001386686.1:c.165+96_165+100del	NP_001373615.1:n.165+96_165+100del
NM_001386687.1:c.165+96_165+100del	NP_001373616.1:n.165+96_165+100del
NM_001386688.1:c.165+96_165+100del	NP_001373617.1:n.165+96_165+100del
NM_001386689.1:c.165+96_165+100del	NP_001373618.1:n.165+96_165+100del
NM_001386690.1:c.165+96_165+100del	NP_001373619.1:n.165+96_165+100del
NM_001386691.1:c.165+96_165+100del	NP_001373620.1:n.165+96_165+100del
NR_170162.1:n.475+96_475+100del
NR_170163.1:n.468+1022_468+1026del