Canonical Allele Identifier: CA6263346

Gene: ACAT1

Linked Data

• dbSNP Id: rs747278765
• ExAC: 11:108016899 GAAC / G
• gnomAD v2: 11-108016899-GAAC-G
• gnomAD v4: 11-108146172-GAAC-G
• MyVariant Identifiers: chr11:g.108016900_108016902del (hg19) ; chr11:g.108146173_108146175del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108146174_108146176del , CM000673.2:g.108146174_108146176del	GRCh38
NC_000011.9:g.108016901_108016903del , CM000673.1:g.108016901_108016903del	GRCh37
NC_000011.8:g.107522111_107522113del	NCBI36
NG_009888.1:g.29644_29646del
NG_009888.2:g.34470_34472del

Transcript Alleles

HGVS	Amino-acid change
ENST00000265838.9:c.1006-28_1006-26del MANE Select	ENSP00000265838.4:n.1006-28_1006-26del
ENST00000671707.1:n.1101-28_1101-26del
ENST00000672031.1:c.941-28_941-26del	ENSP00000500463.1:n.941-28_941-26del
ENST00000672284.1:c.736-28_736-26del	ENSP00000500444.1:n.736-28_736-26del
ENST00000672354.1:c.1006-28_1006-26del	ENSP00000500490.1:n.1006-28_1006-26del
ENST00000672367.1:c.643-28_643-26del	ENSP00000500209.1:n.643-28_643-26del
ENST00000672580.1:c.*261-28_*261-26del	ENSP00000500366.1:n.*261-28_*261-26del
ENST00000672907.1:c.691-28_691-26del	ENSP00000500928.1:n.691-28_691-26del
ENST00000673000.1:n.1094-28_1094-26del
ENST00000673531.1:c.736-28_736-26del	ENSP00000500163.1:n.736-28_736-26del
ENST00000265838.8:c.1006-28_1006-26del	ENSP00000265838.4:n.1006-28_1006-26del
ENST00000533597.1:n.54_56del
NM_000019.3:c.1006-28_1006-26del	NP_000010.1:n.1006-28_1006-26del
XM_006718834.2:c.736-28_736-26del	XP_006718897.1:n.736-28_736-26del
XM_006718835.2:c.736-28_736-26del	XP_006718898.1:n.736-28_736-26del
XM_006718835.3:c.736-28_736-26del	XP_006718898.1:n.736-28_736-26del
XM_017017681.1:c.736-28_736-26del	XP_016873170.1:n.736-28_736-26del
XM_017017682.2:c.628-28_628-26del	XP_016873171.1:n.628-28_628-26del
XM_017017683.2:c.628-28_628-26del	XP_016873172.1:n.628-28_628-26del
XM_024448511.1:c.736-28_736-26del	XP_024304279.1:n.736-28_736-26del
XM_024448512.1:c.736-28_736-26del	XP_024304280.1:n.736-28_736-26del
XM_024448513.1:c.736-28_736-26del	XP_024304281.1:n.736-28_736-26del
XM_024448514.1:c.736-28_736-26del	XP_024304282.1:n.736-28_736-26del
XM_024448515.1:c.736-28_736-26del	XP_024304283.1:n.736-28_736-26del
NM_000019.4:c.1006-28_1006-26del MANE Select	NP_000010.1:n.1006-28_1006-26del
NM_001386677.1:c.1006-28_1006-26del	NP_001373606.1:n.1006-28_1006-26del
NM_001386678.1:c.691-28_691-26del	NP_001373607.1:n.691-28_691-26del
NM_001386679.1:c.709-28_709-26del	NP_001373608.1:n.709-28_709-26del
NM_001386681.1:c.736-28_736-26del	NP_001373610.1:n.736-28_736-26del
NM_001386682.1:c.736-28_736-26del	NP_001373611.1:n.736-28_736-26del
NM_001386685.1:c.736-28_736-26del	NP_001373614.1:n.736-28_736-26del
NM_001386686.1:c.736-28_736-26del	NP_001373615.1:n.736-28_736-26del
NM_001386687.1:c.736-28_736-26del	NP_001373616.1:n.736-28_736-26del
NM_001386688.1:c.736-28_736-26del	NP_001373617.1:n.736-28_736-26del
NM_001386689.1:c.736-28_736-26del	NP_001373618.1:n.736-28_736-26del
NM_001386690.1:c.736-28_736-26del	NP_001373619.1:n.736-28_736-26del
NM_001386691.1:c.736-28_736-26del	NP_001373620.1:n.736-28_736-26del
NR_170162.1:n.981-28_981-26del
NR_170163.1:n.1039-28_1039-26del