Canonical Allele Identifier: CA1998720465

Gene: ACAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108146253A= , CM000673.2:g.108146253A=	GRCh38
NC_000011.9:g.108016980A= , CM000673.1:g.108016980A=	GRCh37
NC_000011.8:g.107522190A=	NCBI36
NG_009888.1:g.29723A=
NG_009888.2:g.34549A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265838.9:c.1057A= MANE Select	ENSP00000265838.4:p.Asn353=
ENST00000671707.1:n.1152A=
ENST00000672031.1:c.*44A=	ENSP00000500463.1:n.*44A=
ENST00000672284.1:c.787A=	ENSP00000500444.1:p.Asn263=
ENST00000672354.1:c.1057A=	ENSP00000500490.1:p.Asn353=
ENST00000672367.1:c.694A=	ENSP00000500209.1:p.Asn232=
ENST00000672580.1:c.*312A=	ENSP00000500366.1:n.*312A=
ENST00000672907.1:c.742A=	ENSP00000500928.1:p.Asn248=
ENST00000673000.1:n.1145A=
ENST00000673531.1:c.787A=	ENSP00000500163.1:p.Asn263=
ENST00000265838.8:c.1057A=	ENSP00000265838.4:p.Asn353=
ENST00000533597.1:n.133A=
NM_000019.3:c.1057A=	NP_000010.1:p.Asn353=
XM_006718834.2:c.787A=	XP_006718897.1:p.Asn263=
XM_006718835.2:c.787A=	XP_006718898.1:p.Asn263=
XM_006718835.3:c.787A=	XP_006718898.1:p.Asn263=
XM_017017681.1:c.787A=	XP_016873170.1:p.Asn263=
XM_017017682.2:c.679A=	XP_016873171.1:p.Asn227=
XM_017017683.2:c.679A=	XP_016873172.1:p.Asn227=
XM_024448511.1:c.787A=	XP_024304279.1:p.Asn263=
XM_024448512.1:c.787A=	XP_024304280.1:p.Asn263=
XM_024448513.1:c.787A=	XP_024304281.1:p.Asn263=
XM_024448514.1:c.787A=	XP_024304282.1:p.Asn263=
XM_024448515.1:c.787A=	XP_024304283.1:p.Asn263=
NM_000019.4:c.1057A= MANE Select	NP_000010.1:p.Asn353=
NM_001386677.1:c.1057A=	NP_001373606.1:p.Asn353=
NM_001386678.1:c.742A=	NP_001373607.1:p.Asn248=
NM_001386679.1:c.760A=	NP_001373608.1:p.Asn254=
NM_001386681.1:c.787A=	NP_001373610.1:p.Asn263=
NM_001386682.1:c.787A=	NP_001373611.1:p.Asn263=
NM_001386685.1:c.787A=	NP_001373614.1:p.Asn263=
NM_001386686.1:c.787A=	NP_001373615.1:p.Asn263=
NM_001386687.1:c.787A=	NP_001373616.1:p.Asn263=
NM_001386688.1:c.787A=	NP_001373617.1:p.Asn263=
NM_001386689.1:c.787A=	NP_001373618.1:p.Asn263=
NM_001386690.1:c.787A=	NP_001373619.1:p.Asn263=
NM_001386691.1:c.787A=	NP_001373620.1:p.Asn263=
NR_170162.1:n.1032A=
NR_170163.1:n.1090A=