Canonical Allele Identifier: CA2062325114

Gene: ACACB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109266520C= , CM000674.2:g.109266520C=	GRCh38
NC_000012.11:g.109704325C= , CM000674.1:g.109704325C=	GRCh37
NC_000012.10:g.108188708C=	NCBI36
NG_046907.1:g.160337C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001093.4:c.*158C= MANE Select	NP_001084.3:n.*158C=
ENST00000338432.12:c.*158C= MANE Select	ENSP00000341044.7:n.*158C=
NM_001093.3:c.*158C=	NP_001084.3:n.*158C=
ENST00000338432.11:c.*158C=	ENSP00000341044.7:n.*158C=
ENST00000377848.7:c.*158C=	ENSP00000367079.3:n.*158C=
ENST00000537279.1:n.1958C=
ENST00000538526.5:c.3619C=
XM_005253876.3:c.*158C=	XP_005253933.1:n.*158C=
XM_005253876.4:c.*158C=	XP_005253933.1:n.*158C=
XM_006719365.2:c.*158C=	XP_006719428.1:n.*158C=
XM_006719367.2:c.*158C=	XP_006719430.1:n.*158C=
XM_006719367.4:c.*158C=	XP_006719430.1:n.*158C=
XM_011538259.1:c.*158C=	XP_011536561.1:n.*158C=
XM_011538259.2:c.*158C=	XP_011536561.1:n.*158C=
XM_011538260.1:c.*158C=	XP_011536562.1:n.*158C=
XM_011538261.1:c.*158C=	XP_011536563.1:n.*158C=
XM_011538262.1:c.*158C=	XP_011536564.1:n.*158C=
XM_011538263.1:c.*158C=	XP_011536565.1:n.*158C=
XM_011538263.3:c.*158C=	XP_011536565.1:n.*158C=
XM_011538264.1:c.*158C=	XP_011536566.1:n.*158C=
XM_011538264.3:c.*158C=	XP_011536566.1:n.*158C=
XM_017019252.2:c.*158C=	XP_016874741.1:n.*158C=
XR_002957320.1:n.8378C=
XR_002957321.1:n.8803C=
XR_002957322.1:n.7690C=
XR_944532.3:n.8306C=