Canonical Allele Identifier: CA382507079

Gene: ACAT1

Linked Data

• MyVariant Identifiers: chr11:g.108009641G>T (hg19) ; chr11:g.108138914G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108138914G>T , CM000673.2:g.108138914G>T	GRCh38
NC_000011.9:g.108009641G>T , CM000673.1:g.108009641G>T	GRCh37
NC_000011.8:g.107514851G>T	NCBI36
NG_009888.1:g.22384G>T
NG_009888.2:g.27210G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265838.9:c.452G>T MANE Select	ENSP00000265838.4:p.Gly151Val
ENST00000671707.1:n.547G>T
ENST00000672008.1:c.*10G>T	ENSP00000500499.1:n.*10G>T
ENST00000672031.1:c.452G>T	ENSP00000500463.1:p.Gly151Val
ENST00000672284.1:c.182G>T	ENSP00000500444.1:p.Gly61Val
ENST00000672354.1:c.452G>T	ENSP00000500490.1:p.Gly151Val
ENST00000672367.1:c.89G>T	ENSP00000500209.1:p.Gly30Val
ENST00000672580.1:c.452G>T	ENSP00000500366.1:p.Gly151Val
ENST00000672907.1:c.137G>T	ENSP00000500928.1:p.Gly46Val
ENST00000673000.1:n.540G>T
ENST00000673531.1:c.182G>T	ENSP00000500163.1:p.Gly61Val
ENST00000265838.8:c.452G>T	ENSP00000265838.4:p.Gly151Val
ENST00000528370.1:c.258G>T
ENST00000531813.5:c.351G>T	ENSP00000435965.1:p.Arg117Ser
ENST00000534773.1:n.195G>T
NM_000019.3:c.452G>T	NP_000010.1:p.Gly151Val
XM_006718834.2:c.182G>T	XP_006718897.1:p.Gly61Val
XM_006718835.2:c.182G>T	XP_006718898.1:p.Gly61Val
XM_006718835.3:c.182G>T	XP_006718898.1:p.Gly61Val
XM_017017681.1:c.182G>T	XP_016873170.1:p.Gly61Val
XM_017017682.2:c.74G>T	XP_016873171.1:p.Gly25Val
XM_017017683.2:c.74G>T	XP_016873172.1:p.Gly25Val
XM_024448511.1:c.182G>T	XP_024304279.1:p.Gly61Val
XM_024448512.1:c.182G>T	XP_024304280.1:p.Gly61Val
XM_024448513.1:c.182G>T	XP_024304281.1:p.Gly61Val
XM_024448514.1:c.182G>T	XP_024304282.1:p.Gly61Val
XM_024448515.1:c.182G>T	XP_024304283.1:p.Gly61Val
NM_000019.4:c.452G>T MANE Select	NP_000010.1:p.Gly151Val
NM_001386677.1:c.452G>T	NP_001373606.1:p.Gly151Val
NM_001386678.1:c.137G>T	NP_001373607.1:p.Gly46Val
NM_001386679.1:c.155G>T	NP_001373608.1:p.Gly52Val
NM_001386681.1:c.182G>T	NP_001373610.1:p.Gly61Val
NM_001386682.1:c.182G>T	NP_001373611.1:p.Gly61Val
NM_001386685.1:c.182G>T	NP_001373614.1:p.Gly61Val
NM_001386686.1:c.182G>T	NP_001373615.1:p.Gly61Val
NM_001386687.1:c.182G>T	NP_001373616.1:p.Gly61Val
NM_001386688.1:c.182G>T	NP_001373617.1:p.Gly61Val
NM_001386689.1:c.182G>T	NP_001373618.1:p.Gly61Val
NM_001386690.1:c.182G>T	NP_001373619.1:p.Gly61Val
NM_001386691.1:c.182G>T	NP_001373620.1:p.Gly61Val
NR_170162.1:n.492G>T
NR_170163.1:n.485G>T