Canonical Allele Identifier: CA601691807

Gene: ACAT1

Linked Data

• dbSNP Id: rs1491157307
• gnomAD v2: 11-108009422-C-CT
• gnomAD v3: 11-108138695-C-CT
• gnomAD v4: 11-108138695-C-CT
• MyVariant Identifiers: chr11:g.108009422_108009423insT (hg19) ; chr11:g.108138695_108138696insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108138695_108138696insT , CM000673.2:g.108138695_108138696insT	GRCh38
NC_000011.9:g.108009422_108009423insT , CM000673.1:g.108009422_108009423insT	GRCh37
NC_000011.8:g.107514632_107514633insT	NCBI36
NG_009888.1:g.22165_22166insT
NG_009888.2:g.26991_26992insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265838.9:c.436-203_436-202insT MANE Select	ENSP00000265838.4:n.436-203_436-202insT
ENST00000671707.1:n.531-203_531-202insT
ENST00000672008.1:c.315-203_315-202insT	ENSP00000500499.1:n.315-203_315-202insT
ENST00000672031.1:c.436-203_436-202insT	ENSP00000500463.1:n.436-203_436-202insT
ENST00000672284.1:c.166-203_166-202insT	ENSP00000500444.1:n.166-203_166-202insT
ENST00000672354.1:c.436-203_436-202insT	ENSP00000500490.1:n.436-203_436-202insT
ENST00000672367.1:c.73-203_73-202insT	ENSP00000500209.1:n.73-203_73-202insT
ENST00000672580.1:c.436-203_436-202insT	ENSP00000500366.1:n.436-203_436-202insT
ENST00000672907.1:c.121-203_121-202insT	ENSP00000500928.1:n.121-203_121-202insT
ENST00000673000.1:n.524-203_524-202insT
ENST00000673531.1:c.166-203_166-202insT	ENSP00000500163.1:n.166-203_166-202insT
ENST00000265838.8:c.436-203_436-202insT	ENSP00000265838.4:n.436-203_436-202insT
ENST00000528370.1:c.242-203_242-202insT
ENST00000531813.5:c.335-203_335-202insT	ENSP00000435965.1:n.335-203_335-202insT
NM_000019.3:c.436-203_436-202insT	NP_000010.1:n.436-203_436-202insT
XM_006718834.2:c.166-203_166-202insT	XP_006718897.1:n.166-203_166-202insT
XM_006718835.2:c.166-203_166-202insT	XP_006718898.1:n.166-203_166-202insT
XM_006718835.3:c.166-203_166-202insT	XP_006718898.1:n.166-203_166-202insT
XM_017017681.1:c.166-203_166-202insT	XP_016873170.1:n.166-203_166-202insT
XM_017017682.2:c.58-203_58-202insT	XP_016873171.1:n.58-203_58-202insT
XM_017017683.2:c.58-203_58-202insT	XP_016873172.1:n.58-203_58-202insT
XM_024448511.1:c.166-203_166-202insT	XP_024304279.1:n.166-203_166-202insT
XM_024448512.1:c.166-203_166-202insT	XP_024304280.1:n.166-203_166-202insT
XM_024448513.1:c.166-203_166-202insT	XP_024304281.1:n.166-203_166-202insT
XM_024448514.1:c.166-203_166-202insT	XP_024304282.1:n.166-203_166-202insT
XM_024448515.1:c.166-203_166-202insT	XP_024304283.1:n.166-203_166-202insT
NM_000019.4:c.436-203_436-202insT MANE Select	NP_000010.1:n.436-203_436-202insT
NM_001386677.1:c.436-203_436-202insT	NP_001373606.1:n.436-203_436-202insT
NM_001386678.1:c.121-203_121-202insT	NP_001373607.1:n.121-203_121-202insT
NM_001386679.1:c.139-203_139-202insT	NP_001373608.1:n.139-203_139-202insT
NM_001386681.1:c.166-203_166-202insT	NP_001373610.1:n.166-203_166-202insT
NM_001386682.1:c.166-203_166-202insT	NP_001373611.1:n.166-203_166-202insT
NM_001386685.1:c.166-203_166-202insT	NP_001373614.1:n.166-203_166-202insT
NM_001386686.1:c.166-203_166-202insT	NP_001373615.1:n.166-203_166-202insT
NM_001386687.1:c.166-203_166-202insT	NP_001373616.1:n.166-203_166-202insT
NM_001386688.1:c.166-203_166-202insT	NP_001373617.1:n.166-203_166-202insT
NM_001386689.1:c.166-203_166-202insT	NP_001373618.1:n.166-203_166-202insT
NM_001386690.1:c.166-203_166-202insT	NP_001373619.1:n.166-203_166-202insT
NM_001386691.1:c.166-203_166-202insT	NP_001373620.1:n.166-203_166-202insT
NR_170162.1:n.476-203_476-202insT
NR_170163.1:n.469-203_469-202insT