Canonical Allele Identifier: CA382508773

Gene: ACAT1

Linked Data

• gnomAD v4: 11-108147311-T-C
• MyVariant Identifiers: chr11:g.108018038T>C (hg19) ; chr11:g.108147311T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108147311T>C , CM000673.2:g.108147311T>C	GRCh38
NC_000011.9:g.108018038T>C , CM000673.1:g.108018038T>C	GRCh37
NC_000011.8:g.107523248T>C	NCBI36
NG_009888.1:g.30781T>C
NG_009888.2:g.35607T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265838.9:c.1205T>C MANE Select	ENSP00000265838.4:p.Leu402Ser
ENST00000671707.1:n.1300T>C
ENST00000672031.1:c.*192T>C	ENSP00000500463.1:n.*192T>C
ENST00000672284.1:c.935T>C	ENSP00000500444.1:p.Leu312Ser
ENST00000672354.1:c.1226T>C	ENSP00000500490.1:p.Leu409Ser
ENST00000672367.1:c.842T>C	ENSP00000500209.1:p.Leu281Ser
ENST00000672580.1:c.*460T>C	ENSP00000500366.1:n.*460T>C
ENST00000672907.1:c.890T>C	ENSP00000500928.1:p.Leu297Ser
ENST00000673000.1:n.1293T>C
ENST00000673531.1:c.935T>C	ENSP00000500163.1:p.Leu312Ser
ENST00000265838.8:c.1205T>C	ENSP00000265838.4:p.Leu402Ser
ENST00000533597.1:n.281T>C
NM_000019.3:c.1205T>C	NP_000010.1:p.Leu402Ser
XM_006718834.2:c.935T>C	XP_006718897.1:p.Leu312Ser
XM_006718835.2:c.935T>C	XP_006718898.1:p.Leu312Ser
XM_006718835.3:c.935T>C	XP_006718898.1:p.Leu312Ser
XM_017017681.1:c.935T>C	XP_016873170.1:p.Leu312Ser
XM_017017682.2:c.827T>C	XP_016873171.1:p.Leu276Ser
XM_017017683.2:c.827T>C	XP_016873172.1:p.Leu276Ser
XM_024448511.1:c.935T>C	XP_024304279.1:p.Leu312Ser
XM_024448512.1:c.935T>C	XP_024304280.1:p.Leu312Ser
XM_024448513.1:c.935T>C	XP_024304281.1:p.Leu312Ser
XM_024448514.1:c.935T>C	XP_024304282.1:p.Leu312Ser
XM_024448515.1:c.935T>C	XP_024304283.1:p.Leu312Ser
NM_000019.4:c.1205T>C MANE Select	NP_000010.1:p.Leu402Ser
NM_001386677.1:c.1226T>C	NP_001373606.1:p.Leu409Ser
NM_001386678.1:c.890T>C	NP_001373607.1:p.Leu297Ser
NM_001386679.1:c.908T>C	NP_001373608.1:p.Leu303Ser
NM_001386681.1:c.935T>C	NP_001373610.1:p.Leu312Ser
NM_001386682.1:c.935T>C	NP_001373611.1:p.Leu312Ser
NM_001386685.1:c.935T>C	NP_001373614.1:p.Leu312Ser
NM_001386686.1:c.935T>C	NP_001373615.1:p.Leu312Ser
NM_001386687.1:c.935T>C	NP_001373616.1:p.Leu312Ser
NM_001386688.1:c.935T>C	NP_001373617.1:p.Leu312Ser
NM_001386689.1:c.935T>C	NP_001373618.1:p.Leu312Ser
NM_001386690.1:c.935T>C	NP_001373619.1:p.Leu312Ser
NM_001386691.1:c.935T>C	NP_001373620.1:p.Leu312Ser
NR_170162.1:n.1180T>C
NR_170163.1:n.1238T>C