Canonical Allele Identifier: CA228359111

Gene: ACAT1

Linked Data

• dbSNP Id: rs757296238
• gnomAD v4: 11-108147134-T-TA
• MyVariant Identifiers: chr11:g.108017861_108017862insA (hg19) ; chr11:g.108147134_108147135insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108147134_108147135insA , CM000673.2:g.108147134_108147135insA	GRCh38
NC_000011.9:g.108017861_108017862insA , CM000673.1:g.108017861_108017862insA	GRCh37
NC_000011.8:g.107523071_107523072insA	NCBI36
NG_009888.1:g.30604_30605insA
NG_009888.2:g.35430_35431insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265838.9:c.1164-136_1164-135insA MANE Select	ENSP00000265838.4:n.1164-136_1164-135insA
ENST00000671707.1:n.1259-136_1259-135insA
ENST00000672031.1:c.*151-136_*151-135insA	ENSP00000500463.1:n.*151-136_*151-135insA
ENST00000672284.1:c.894-136_894-135insA	ENSP00000500444.1:n.894-136_894-135insA
ENST00000672354.1:c.1164-115_1164-114insA	ENSP00000500490.1:n.1164-115_1164-114insA
ENST00000672367.1:c.801-136_801-135insA	ENSP00000500209.1:n.801-136_801-135insA
ENST00000672580.1:c.*419-136_*419-135insA	ENSP00000500366.1:n.*419-136_*419-135insA
ENST00000672907.1:c.849-136_849-135insA	ENSP00000500928.1:n.849-136_849-135insA
ENST00000673000.1:n.1252-136_1252-135insA
ENST00000673531.1:c.894-136_894-135insA	ENSP00000500163.1:n.894-136_894-135insA
ENST00000265838.8:c.1164-136_1164-135insA	ENSP00000265838.4:n.1164-136_1164-135insA
ENST00000533597.1:n.240-136_240-135insA
NM_000019.3:c.1164-136_1164-135insA	NP_000010.1:n.1164-136_1164-135insA
XM_006718834.2:c.894-136_894-135insA	XP_006718897.1:n.894-136_894-135insA
XM_006718835.2:c.894-136_894-135insA	XP_006718898.1:n.894-136_894-135insA
XM_006718835.3:c.894-136_894-135insA	XP_006718898.1:n.894-136_894-135insA
XM_017017681.1:c.894-136_894-135insA	XP_016873170.1:n.894-136_894-135insA
XM_017017682.2:c.786-136_786-135insA	XP_016873171.1:n.786-136_786-135insA
XM_017017683.2:c.786-136_786-135insA	XP_016873172.1:n.786-136_786-135insA
XM_024448511.1:c.894-136_894-135insA	XP_024304279.1:n.894-136_894-135insA
XM_024448512.1:c.894-136_894-135insA	XP_024304280.1:n.894-136_894-135insA
XM_024448513.1:c.894-136_894-135insA	XP_024304281.1:n.894-136_894-135insA
XM_024448514.1:c.894-136_894-135insA	XP_024304282.1:n.894-136_894-135insA
XM_024448515.1:c.894-136_894-135insA	XP_024304283.1:n.894-136_894-135insA
NM_000019.4:c.1164-136_1164-135insA MANE Select	NP_000010.1:n.1164-136_1164-135insA
NM_001386677.1:c.1164-115_1164-114insA	NP_001373606.1:n.1164-115_1164-114insA
NM_001386678.1:c.849-136_849-135insA	NP_001373607.1:n.849-136_849-135insA
NM_001386679.1:c.867-136_867-135insA	NP_001373608.1:n.867-136_867-135insA
NM_001386681.1:c.894-136_894-135insA	NP_001373610.1:n.894-136_894-135insA
NM_001386682.1:c.894-136_894-135insA	NP_001373611.1:n.894-136_894-135insA
NM_001386685.1:c.894-136_894-135insA	NP_001373614.1:n.894-136_894-135insA
NM_001386686.1:c.894-136_894-135insA	NP_001373615.1:n.894-136_894-135insA
NM_001386687.1:c.894-136_894-135insA	NP_001373616.1:n.894-136_894-135insA
NM_001386688.1:c.894-136_894-135insA	NP_001373617.1:n.894-136_894-135insA
NM_001386689.1:c.894-136_894-135insA	NP_001373618.1:n.894-136_894-135insA
NM_001386690.1:c.894-136_894-135insA	NP_001373619.1:n.894-136_894-135insA
NM_001386691.1:c.894-136_894-135insA	NP_001373620.1:n.894-136_894-135insA
NR_170162.1:n.1139-136_1139-135insA
NR_170163.1:n.1197-136_1197-135insA