Canonical Allele Identifier: CA6263089

Gene: ACAT1

Linked Data

• dbSNP Id: rs771084397
• ExAC: 11:108005838 GTT / G
• gnomAD v2: 11-108005838-GTT-G
• gnomAD v3: 11-108135111-GTT-G
• gnomAD v4: 11-108135111-GTT-G
• MyVariant Identifiers: chr11:g.108005839_108005840del (hg19) ; chr11:g.108135112_108135113del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108135115_108135116del , CM000673.2:g.108135115_108135116del	GRCh38
NC_000011.9:g.108005842_108005843del , CM000673.1:g.108005842_108005843del	GRCh37
NC_000011.8:g.107511052_107511053del	NCBI36
NG_009888.1:g.18585_18586del
NG_009888.2:g.23411_23412del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265838.9:c.335-27_335-26del MANE Select	ENSP00000265838.4:n.335-27_335-26del
ENST00000671707.1:n.430-27_430-26del
ENST00000672008.1:c.314+819_314+820del	ENSP00000500499.1:n.314+819_314+820del
ENST00000672031.1:c.335-27_335-26del	ENSP00000500463.1:n.335-27_335-26del
ENST00000672284.1:c.65-27_65-26del	ENSP00000500444.1:n.65-27_65-26del
ENST00000672354.1:c.335-27_335-26del	ENSP00000500490.1:n.335-27_335-26del
ENST00000672367.1:c.73-3783_73-3782del	ENSP00000500209.1:n.73-3783_73-3782del
ENST00000672580.1:c.335-27_335-26del	ENSP00000500366.1:n.335-27_335-26del
ENST00000672907.1:c.120+3161_120+3162del	ENSP00000500928.1:n.120+3161_120+3162del
ENST00000673000.1:n.423-27_423-26del
ENST00000673531.1:c.65-27_65-26del	ENSP00000500163.1:n.65-27_65-26del
ENST00000265838.8:c.335-27_335-26del	ENSP00000265838.4:n.335-27_335-26del
ENST00000299355.10:c.335-27_335-26del	ENSP00000299355.6:n.335-27_335-26del
ENST00000527942.5:c.65-27_65-26del	ENSP00000433568.1:n.65-27_65-26del
ENST00000528370.1:c.141-27_141-26del
ENST00000531813.5:c.334+799_334+800del	ENSP00000435965.1:n.334+799_334+800del
NM_000019.3:c.335-27_335-26del	NP_000010.1:n.335-27_335-26del
XM_006718834.2:c.65-27_65-26del	XP_006718897.1:n.65-27_65-26del
XM_006718835.2:c.65-27_65-26del	XP_006718898.1:n.65-27_65-26del
XM_006718835.3:c.65-27_65-26del	XP_006718898.1:n.65-27_65-26del
XM_017017681.1:c.65-27_65-26del	XP_016873170.1:n.65-27_65-26del
XM_017017682.2:c.57+799_57+800del	XP_016873171.1:n.57+799_57+800del
XM_017017683.2:c.57+799_57+800del	XP_016873172.1:n.57+799_57+800del
XM_024448511.1:c.65-27_65-26del	XP_024304279.1:n.65-27_65-26del
XM_024448512.1:c.65-27_65-26del	XP_024304280.1:n.65-27_65-26del
XM_024448513.1:c.65-27_65-26del	XP_024304281.1:n.65-27_65-26del
XM_024448514.1:c.65-27_65-26del	XP_024304282.1:n.65-27_65-26del
XM_024448515.1:c.65-27_65-26del	XP_024304283.1:n.65-27_65-26del
NM_000019.4:c.335-27_335-26del MANE Select	NP_000010.1:n.335-27_335-26del
NM_001386677.1:c.335-27_335-26del	NP_001373606.1:n.335-27_335-26del
NM_001386678.1:c.120+3161_120+3162del	NP_001373607.1:n.120+3161_120+3162del
NM_001386679.1:c.38-27_38-26del	NP_001373608.1:n.38-27_38-26del
NM_001386681.1:c.65-27_65-26del	NP_001373610.1:n.65-27_65-26del
NM_001386682.1:c.65-27_65-26del	NP_001373611.1:n.65-27_65-26del
NM_001386685.1:c.65-27_65-26del	NP_001373614.1:n.65-27_65-26del
NM_001386686.1:c.65-27_65-26del	NP_001373615.1:n.65-27_65-26del
NM_001386687.1:c.65-27_65-26del	NP_001373616.1:n.65-27_65-26del
NM_001386688.1:c.65-27_65-26del	NP_001373617.1:n.65-27_65-26del
NM_001386689.1:c.65-27_65-26del	NP_001373618.1:n.65-27_65-26del
NM_001386690.1:c.65-27_65-26del	NP_001373619.1:n.65-27_65-26del
NM_001386691.1:c.65-27_65-26del	NP_001373620.1:n.65-27_65-26del
NR_170162.1:n.375-27_375-26del
NR_170163.1:n.468+799_468+800del