Canonical Allele Identifier: CA2062308027

Gene: ACACB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109217349T= , CM000674.2:g.109217349T=	GRCh38
NC_000012.11:g.109655154T= , CM000674.1:g.109655154T=	GRCh37
NC_000012.10:g.108139537T=	NCBI36
NG_046907.1:g.111166T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338432.12:c.3564+429T= MANE Select	ENSP00000341044.7:n.3564+429T=
ENST00000338432.11:c.3564+429T=	ENSP00000341044.7:n.3564+429T=
ENST00000377848.7:c.3564+429T=	ENSP00000367079.3:n.3564+429T=
ENST00000377854.9:c.-439+429T=	ENSP00000367085.6:n.-439+429T=
NM_001093.3:c.3564+429T=	NP_001084.3:n.3564+429T=
XM_005253876.3:c.3564+429T=	XP_005253933.1:n.3564+429T=
XM_006719365.2:c.3564+429T=	XP_006719428.1:n.3564+429T=
XM_006719367.2:c.2958+429T=	XP_006719430.1:n.2958+429T=
XM_011538259.1:c.3564+429T=	XP_011536561.1:n.3564+429T=
XM_011538260.1:c.3564+429T=	XP_011536562.1:n.3564+429T=
XM_011538261.1:c.3564+429T=	XP_011536563.1:n.3564+429T=
XM_011538262.1:c.3564+429T=	XP_011536564.1:n.3564+429T=
XM_011538263.1:c.3375+429T=	XP_011536565.1:n.3375+429T=
XM_011538264.1:c.2937+429T=	XP_011536566.1:n.2937+429T=
XM_011538265.1:c.3564+429T=	XP_011536567.1:n.3564+429T=
XR_944530.1:n.4311+429T=
XR_944531.1:n.4311+429T=
XR_944532.1:n.4311+429T=
XR_944533.1:n.4312+429T=
XM_005253876.4:c.3564+429T=	XP_005253933.1:n.3564+429T=
XM_006719367.4:c.2958+429T=	XP_006719430.1:n.2958+429T=
XM_011538259.2:c.3564+429T=	XP_011536561.1:n.3564+429T=
XM_011538263.3:c.3375+429T=	XP_011536565.1:n.3375+429T=
XM_011538264.3:c.2937+429T=	XP_011536566.1:n.2937+429T=
XM_011538265.2:c.3564+429T=	XP_011536567.1:n.3564+429T=
XM_017019252.2:c.2769+429T=	XP_016874741.1:n.2769+429T=
XR_002957320.1:n.4322+429T=
XR_002957321.1:n.4322+429T=
XR_002957322.1:n.3209+429T=
XR_944530.2:n.4322+429T=
XR_944532.3:n.4322+429T=
NM_001093.4:c.3564+429T= MANE Select	NP_001084.3:n.3564+429T=