Canonical Allele Identifier: CA1998718281

Gene: ACAT1

Linked Data

• dbSNP Id: rs2077585194
• gnomAD v4: 11-108141510-AAGGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108141514_108141517del , CM000673.2:g.108141514_108141517del	GRCh38
NC_000011.9:g.108012241_108012244del , CM000673.1:g.108012241_108012244del	GRCh37
NC_000011.8:g.107517451_107517454del	NCBI36
NG_009888.1:g.24984_24987del
NG_009888.2:g.29810_29813del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265838.9:c.731-91_731-88del MANE Select	ENSP00000265838.4:n.731-91_731-88del
ENST00000671707.1:n.826-91_826-88del
ENST00000672008.1:c.*289-91_*289-88del	ENSP00000500499.1:n.*289-91_*289-88del
ENST00000672031.1:c.731-91_731-88del	ENSP00000500463.1:n.731-91_731-88del
ENST00000672284.1:c.461-91_461-88del	ENSP00000500444.1:n.461-91_461-88del
ENST00000672354.1:c.731-91_731-88del	ENSP00000500490.1:n.731-91_731-88del
ENST00000672367.1:c.368-91_368-88del	ENSP00000500209.1:n.368-91_368-88del
ENST00000672580.1:c.580-91_580-88del	ENSP00000500366.1:n.580-91_580-88del
ENST00000672907.1:c.416-91_416-88del	ENSP00000500928.1:n.416-91_416-88del
ENST00000673000.1:n.819-91_819-88del
ENST00000673531.1:c.461-91_461-88del	ENSP00000500163.1:n.461-91_461-88del
ENST00000265838.8:c.731-91_731-88del	ENSP00000265838.4:n.731-91_731-88del
ENST00000531813.5:c.*204-91_*204-88del	ENSP00000435965.1:n.*204-91_*204-88del
ENST00000532792.5:n.226-91_226-88del
ENST00000533610.1:n.192-91_192-88del
NM_000019.3:c.731-91_731-88del	NP_000010.1:n.731-91_731-88del
XM_006718834.2:c.461-91_461-88del	XP_006718897.1:n.461-91_461-88del
XM_006718835.2:c.461-91_461-88del	XP_006718898.1:n.461-91_461-88del
XM_006718835.3:c.461-91_461-88del	XP_006718898.1:n.461-91_461-88del
XM_017017681.1:c.461-91_461-88del	XP_016873170.1:n.461-91_461-88del
XM_017017682.2:c.353-91_353-88del	XP_016873171.1:n.353-91_353-88del
XM_017017683.2:c.353-91_353-88del	XP_016873172.1:n.353-91_353-88del
XM_024448511.1:c.461-91_461-88del	XP_024304279.1:n.461-91_461-88del
XM_024448512.1:c.461-91_461-88del	XP_024304280.1:n.461-91_461-88del
XM_024448513.1:c.461-91_461-88del	XP_024304281.1:n.461-91_461-88del
XM_024448514.1:c.461-91_461-88del	XP_024304282.1:n.461-91_461-88del
XM_024448515.1:c.461-91_461-88del	XP_024304283.1:n.461-91_461-88del
NM_000019.4:c.731-91_731-88del MANE Select	NP_000010.1:n.731-91_731-88del
NM_001386677.1:c.731-91_731-88del	NP_001373606.1:n.731-91_731-88del
NM_001386678.1:c.416-91_416-88del	NP_001373607.1:n.416-91_416-88del
NM_001386679.1:c.434-91_434-88del	NP_001373608.1:n.434-91_434-88del
NM_001386681.1:c.461-91_461-88del	NP_001373610.1:n.461-91_461-88del
NM_001386682.1:c.461-91_461-88del	NP_001373611.1:n.461-91_461-88del
NM_001386685.1:c.461-91_461-88del	NP_001373614.1:n.461-91_461-88del
NM_001386686.1:c.461-91_461-88del	NP_001373615.1:n.461-91_461-88del
NM_001386687.1:c.461-91_461-88del	NP_001373616.1:n.461-91_461-88del
NM_001386688.1:c.461-91_461-88del	NP_001373617.1:n.461-91_461-88del
NM_001386689.1:c.461-91_461-88del	NP_001373618.1:n.461-91_461-88del
NM_001386690.1:c.461-91_461-88del	NP_001373619.1:n.461-91_461-88del
NM_001386691.1:c.461-91_461-88del	NP_001373620.1:n.461-91_461-88del
NR_170162.1:n.771-91_771-88del
NR_170163.1:n.764-91_764-88del