Canonical Allele Identifier: CA382507069

Gene: ACAT1

Linked Data

• MyVariant Identifiers: chr11:g.108009637G>A (hg19) ; chr11:g.108138910G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108138910G>A , CM000673.2:g.108138910G>A	GRCh38
NC_000011.9:g.108009637G>A , CM000673.1:g.108009637G>A	GRCh37
NC_000011.8:g.107514847G>A	NCBI36
NG_009888.1:g.22380G>A
NG_009888.2:g.27206G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265838.9:c.448G>A MANE Select	ENSP00000265838.4:p.Ala150Thr
ENST00000671707.1:n.543G>A
ENST00000672008.1:c.*6G>A	ENSP00000500499.1:n.*6G>A
ENST00000672031.1:c.448G>A	ENSP00000500463.1:p.Ala150Thr
ENST00000672284.1:c.178G>A	ENSP00000500444.1:p.Ala60Thr
ENST00000672354.1:c.448G>A	ENSP00000500490.1:p.Ala150Thr
ENST00000672367.1:c.85G>A	ENSP00000500209.1:p.Ala29Thr
ENST00000672580.1:c.448G>A	ENSP00000500366.1:p.Ala150Thr
ENST00000672907.1:c.133G>A	ENSP00000500928.1:p.Ala45Thr
ENST00000673000.1:n.536G>A
ENST00000673531.1:c.178G>A	ENSP00000500163.1:p.Ala60Thr
ENST00000265838.8:c.448G>A	ENSP00000265838.4:p.Ala150Thr
ENST00000528370.1:c.254G>A
ENST00000531813.5:c.347G>A	ENSP00000435965.1:p.Gly116Asp
ENST00000534773.1:n.191G>A
NM_000019.3:c.448G>A	NP_000010.1:p.Ala150Thr
XM_006718834.2:c.178G>A	XP_006718897.1:p.Ala60Thr
XM_006718835.2:c.178G>A	XP_006718898.1:p.Ala60Thr
XM_006718835.3:c.178G>A	XP_006718898.1:p.Ala60Thr
XM_017017681.1:c.178G>A	XP_016873170.1:p.Ala60Thr
XM_017017682.2:c.70G>A	XP_016873171.1:p.Ala24Thr
XM_017017683.2:c.70G>A	XP_016873172.1:p.Ala24Thr
XM_024448511.1:c.178G>A	XP_024304279.1:p.Ala60Thr
XM_024448512.1:c.178G>A	XP_024304280.1:p.Ala60Thr
XM_024448513.1:c.178G>A	XP_024304281.1:p.Ala60Thr
XM_024448514.1:c.178G>A	XP_024304282.1:p.Ala60Thr
XM_024448515.1:c.178G>A	XP_024304283.1:p.Ala60Thr
NM_000019.4:c.448G>A MANE Select	NP_000010.1:p.Ala150Thr
NM_001386677.1:c.448G>A	NP_001373606.1:p.Ala150Thr
NM_001386678.1:c.133G>A	NP_001373607.1:p.Ala45Thr
NM_001386679.1:c.151G>A	NP_001373608.1:p.Ala51Thr
NM_001386681.1:c.178G>A	NP_001373610.1:p.Ala60Thr
NM_001386682.1:c.178G>A	NP_001373611.1:p.Ala60Thr
NM_001386685.1:c.178G>A	NP_001373614.1:p.Ala60Thr
NM_001386686.1:c.178G>A	NP_001373615.1:p.Ala60Thr
NM_001386687.1:c.178G>A	NP_001373616.1:p.Ala60Thr
NM_001386688.1:c.178G>A	NP_001373617.1:p.Ala60Thr
NM_001386689.1:c.178G>A	NP_001373618.1:p.Ala60Thr
NM_001386690.1:c.178G>A	NP_001373619.1:p.Ala60Thr
NM_001386691.1:c.178G>A	NP_001373620.1:p.Ala60Thr
NR_170162.1:n.488G>A
NR_170163.1:n.481G>A