Canonical Allele Identifier: CA476672011

Gene: ACAT1

Linked Data

• MyVariant Identifiers: chr11:g.108005951T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108135224T>C , CM000673.2:g.108135224T>C	GRCh38
NC_000011.9:g.108005951T>C , CM000673.1:g.108005951T>C	GRCh37
NC_000011.8:g.107511161T>C	NCBI36
NG_009888.1:g.18694T>C
NG_009888.2:g.23520T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265838.9:c.417T>C MANE Select	ENSP00000265838.4:p.Ser139=
ENST00000671707.1:n.512T>C
ENST00000672008.1:c.314+928T>C	ENSP00000500499.1:n.314+928T>C
ENST00000672031.1:c.417T>C	ENSP00000500463.1:p.Ser139=
ENST00000672284.1:c.147T>C	ENSP00000500444.1:p.Ser49=
ENST00000672354.1:c.417T>C	ENSP00000500490.1:p.Ser139=
ENST00000672367.1:c.73-3674T>C	ENSP00000500209.1:n.73-3674T>C
ENST00000672580.1:c.417T>C	ENSP00000500366.1:p.Ser139=
ENST00000672907.1:c.120+3270T>C	ENSP00000500928.1:n.120+3270T>C
ENST00000673000.1:n.505T>C
ENST00000673531.1:c.147T>C	ENSP00000500163.1:p.Ser49=
ENST00000265838.8:c.417T>C	ENSP00000265838.4:p.Ser139=
ENST00000299355.10:c.417T>C	ENSP00000299355.6:p.Ser139=
ENST00000527942.5:c.147T>C	ENSP00000433568.1:p.Ser49=
ENST00000528370.1:c.223T>C
ENST00000531813.5:c.334+908T>C	ENSP00000435965.1:n.334+908T>C
NM_000019.3:c.417T>C	NP_000010.1:p.Ser139=
XM_006718834.2:c.147T>C	XP_006718897.1:p.Ser49=
XM_006718835.2:c.147T>C	XP_006718898.1:p.Ser49=
XM_006718835.3:c.147T>C	XP_006718898.1:p.Ser49=
XM_017017681.1:c.147T>C	XP_016873170.1:p.Ser49=
XM_017017682.2:c.57+908T>C	XP_016873171.1:n.57+908T>C
XM_017017683.2:c.57+908T>C	XP_016873172.1:n.57+908T>C
XM_024448511.1:c.147T>C	XP_024304279.1:p.Ser49=
XM_024448512.1:c.147T>C	XP_024304280.1:p.Ser49=
XM_024448513.1:c.147T>C	XP_024304281.1:p.Ser49=
XM_024448514.1:c.147T>C	XP_024304282.1:p.Ser49=
XM_024448515.1:c.147T>C	XP_024304283.1:p.Ser49=
NM_000019.4:c.417T>C MANE Select	NP_000010.1:p.Ser139=
NM_001386677.1:c.417T>C	NP_001373606.1:p.Ser139=
NM_001386678.1:c.120+3270T>C	NP_001373607.1:n.120+3270T>C
NM_001386679.1:c.120T>C	NP_001373608.1:p.Ser40=
NM_001386681.1:c.147T>C	NP_001373610.1:p.Ser49=
NM_001386682.1:c.147T>C	NP_001373611.1:p.Ser49=
NM_001386685.1:c.147T>C	NP_001373614.1:p.Ser49=
NM_001386686.1:c.147T>C	NP_001373615.1:p.Ser49=
NM_001386687.1:c.147T>C	NP_001373616.1:p.Ser49=
NM_001386688.1:c.147T>C	NP_001373617.1:p.Ser49=
NM_001386689.1:c.147T>C	NP_001373618.1:p.Ser49=
NM_001386690.1:c.147T>C	NP_001373619.1:p.Ser49=
NM_001386691.1:c.147T>C	NP_001373620.1:p.Ser49=
NR_170162.1:n.457T>C
NR_170163.1:n.468+908T>C