Canonical Allele Identifier: CA382508484

Gene: ACAT1

Linked Data

• dbSNP Id: rs1591374644
• gnomAD v4: 11-108146268-C-G
• MyVariant Identifiers: chr11:g.108016995C>G (hg19) ; chr11:g.108146268C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108146268C>G , CM000673.2:g.108146268C>G	GRCh38
NC_000011.9:g.108016995C>G , CM000673.1:g.108016995C>G	GRCh37
NC_000011.8:g.107522205C>G	NCBI36
NG_009888.1:g.29738C>G
NG_009888.2:g.34564C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265838.9:c.1072C>G MANE Select	ENSP00000265838.4:p.Leu358Val
ENST00000671707.1:n.1167C>G
ENST00000672031.1:c.*59C>G	ENSP00000500463.1:n.*59C>G
ENST00000672284.1:c.802C>G	ENSP00000500444.1:p.Leu268Val
ENST00000672354.1:c.1072C>G	ENSP00000500490.1:p.Leu358Val
ENST00000672367.1:c.709C>G	ENSP00000500209.1:p.Leu237Val
ENST00000672580.1:c.*327C>G	ENSP00000500366.1:n.*327C>G
ENST00000672907.1:c.757C>G	ENSP00000500928.1:p.Leu253Val
ENST00000673000.1:n.1160C>G
ENST00000673531.1:c.802C>G	ENSP00000500163.1:p.Leu268Val
ENST00000265838.8:c.1072C>G	ENSP00000265838.4:p.Leu358Val
ENST00000533597.1:n.148C>G
NM_000019.3:c.1072C>G	NP_000010.1:p.Leu358Val
XM_006718834.2:c.802C>G	XP_006718897.1:p.Leu268Val
XM_006718835.2:c.802C>G	XP_006718898.1:p.Leu268Val
XM_006718835.3:c.802C>G	XP_006718898.1:p.Leu268Val
XM_017017681.1:c.802C>G	XP_016873170.1:p.Leu268Val
XM_017017682.2:c.694C>G	XP_016873171.1:p.Leu232Val
XM_017017683.2:c.694C>G	XP_016873172.1:p.Leu232Val
XM_024448511.1:c.802C>G	XP_024304279.1:p.Leu268Val
XM_024448512.1:c.802C>G	XP_024304280.1:p.Leu268Val
XM_024448513.1:c.802C>G	XP_024304281.1:p.Leu268Val
XM_024448514.1:c.802C>G	XP_024304282.1:p.Leu268Val
XM_024448515.1:c.802C>G	XP_024304283.1:p.Leu268Val
NM_000019.4:c.1072C>G MANE Select	NP_000010.1:p.Leu358Val
NM_001386677.1:c.1072C>G	NP_001373606.1:p.Leu358Val
NM_001386678.1:c.757C>G	NP_001373607.1:p.Leu253Val
NM_001386679.1:c.775C>G	NP_001373608.1:p.Leu259Val
NM_001386681.1:c.802C>G	NP_001373610.1:p.Leu268Val
NM_001386682.1:c.802C>G	NP_001373611.1:p.Leu268Val
NM_001386685.1:c.802C>G	NP_001373614.1:p.Leu268Val
NM_001386686.1:c.802C>G	NP_001373615.1:p.Leu268Val
NM_001386687.1:c.802C>G	NP_001373616.1:p.Leu268Val
NM_001386688.1:c.802C>G	NP_001373617.1:p.Leu268Val
NM_001386689.1:c.802C>G	NP_001373618.1:p.Leu268Val
NM_001386690.1:c.802C>G	NP_001373619.1:p.Leu268Val
NM_001386691.1:c.802C>G	NP_001373620.1:p.Leu268Val
NR_170162.1:n.1047C>G
NR_170163.1:n.1105C>G