Canonical Allele Identifier: CA6263243

Gene: ACAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108142501G>A , CM000673.2:g.108142501G>A	GRCh38
NC_000011.9:g.108013228G>A , CM000673.1:g.108013228G>A	GRCh37
NC_000011.8:g.107518438G>A	NCBI36
NG_009888.1:g.25971G>A
NG_009888.2:g.30797G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000019.4:c.891G>A MANE Select	NP_000010.1:p.Thr297=
ENST00000265838.9:c.891G>A MANE Select	ENSP00000265838.4:p.Thr297=
NM_000019.3:c.891G>A	NP_000010.1:p.Thr297=
NM_001386677.1:c.891G>A	NP_001373606.1:p.Thr297=
NM_001386678.1:c.576G>A	NP_001373607.1:p.Thr192=
NM_001386679.1:c.594G>A	NP_001373608.1:p.Thr198=
NM_001386681.1:c.621G>A	NP_001373610.1:p.Thr207=
NM_001386682.1:c.621G>A	NP_001373611.1:p.Thr207=
NM_001386685.1:c.621G>A	NP_001373614.1:p.Thr207=
NM_001386686.1:c.621G>A	NP_001373615.1:p.Thr207=
NM_001386687.1:c.621G>A	NP_001373616.1:p.Thr207=
NM_001386688.1:c.621G>A	NP_001373617.1:p.Thr207=
NM_001386689.1:c.621G>A	NP_001373618.1:p.Thr207=
NM_001386690.1:c.621G>A	NP_001373619.1:p.Thr207=
NM_001386691.1:c.621G>A	NP_001373620.1:p.Thr207=
NR_170162.1:n.931G>A
NR_170163.1:n.924G>A
ENST00000265838.8:c.891G>A	ENSP00000265838.4:p.Thr297=
ENST00000531813.5:c.*364G>A	ENSP00000435965.1:n.*364G>A
ENST00000532792.5:n.386G>A
ENST00000533610.1:n.352G>A
ENST00000671707.1:n.986G>A
ENST00000672031.1:c.891G>A	ENSP00000500463.1:p.Thr297=
ENST00000672284.1:c.621G>A	ENSP00000500444.1:p.Thr207=
ENST00000672354.1:c.891G>A	ENSP00000500490.1:p.Thr297=
ENST00000672367.1:c.528G>A	ENSP00000500209.1:p.Thr176=
ENST00000672580.1:c.*146G>A	ENSP00000500366.1:n.*146G>A
ENST00000672907.1:c.576G>A	ENSP00000500928.1:p.Thr192=
ENST00000673000.1:n.979G>A
ENST00000673531.1:c.621G>A	ENSP00000500163.1:p.Thr207=
XM_006718834.2:c.621G>A	XP_006718897.1:p.Thr207=
XM_006718835.2:c.621G>A	XP_006718898.1:p.Thr207=
XM_006718835.3:c.621G>A	XP_006718898.1:p.Thr207=
XM_017017681.1:c.621G>A	XP_016873170.1:p.Thr207=
XM_017017682.2:c.513G>A	XP_016873171.1:p.Thr171=
XM_017017683.2:c.513G>A	XP_016873172.1:p.Thr171=
XM_024448511.1:c.621G>A	XP_024304279.1:p.Thr207=
XM_024448512.1:c.621G>A	XP_024304280.1:p.Thr207=
XM_024448513.1:c.621G>A	XP_024304281.1:p.Thr207=
XM_024448514.1:c.621G>A	XP_024304282.1:p.Thr207=
XM_024448515.1:c.621G>A	XP_024304283.1:p.Thr207=