Canonical Allele Identifier: CA683386701

Gene: ACACB

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109205890A>T , CM000674.2:g.109205890A>T	GRCh38
NC_000012.11:g.109643695A>T , CM000674.1:g.109643695A>T	GRCh37
NC_000012.10:g.108128078A>T	NCBI36
NG_046907.1:g.99707A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338432.12:c.2914-820A>T MANE Select	ENSP00000341044.7:n.2914-820A>T
ENST00000338432.11:c.2914-820A>T	ENSP00000341044.7:n.2914-820A>T
ENST00000377848.7:c.2914-820A>T	ENSP00000367079.3:n.2914-820A>T
ENST00000377854.9:c.-1089-820A>T	ENSP00000367085.6:n.-1089-820A>T
NM_001093.3:c.2914-820A>T	NP_001084.3:n.2914-820A>T
XM_005253876.3:c.2914-820A>T	XP_005253933.1:n.2914-820A>T
XM_006719365.2:c.2914-820A>T	XP_006719428.1:n.2914-820A>T
XM_006719367.2:c.2308-820A>T	XP_006719430.1:n.2308-820A>T
XM_011538259.1:c.2914-820A>T	XP_011536561.1:n.2914-820A>T
XM_011538260.1:c.2914-820A>T	XP_011536562.1:n.2914-820A>T
XM_011538261.1:c.2914-820A>T	XP_011536563.1:n.2914-820A>T
XM_011538262.1:c.2914-820A>T	XP_011536564.1:n.2914-820A>T
XM_011538263.1:c.2914-820A>T	XP_011536565.1:n.2914-820A>T
XM_011538264.1:c.2287-820A>T	XP_011536566.1:n.2287-820A>T
XM_011538265.1:c.2914-820A>T	XP_011536567.1:n.2914-820A>T
XR_944530.1:n.3661-820A>T
XR_944531.1:n.3661-820A>T
XR_944532.1:n.3661-820A>T
XR_944533.1:n.3662-820A>T
XM_005253876.4:c.2914-820A>T	XP_005253933.1:n.2914-820A>T
XM_006719367.4:c.2308-820A>T	XP_006719430.1:n.2308-820A>T
XM_011538259.2:c.2914-820A>T	XP_011536561.1:n.2914-820A>T
XM_011538263.3:c.2914-820A>T	XP_011536565.1:n.2914-820A>T
XM_011538264.3:c.2287-820A>T	XP_011536566.1:n.2287-820A>T
XM_011538265.2:c.2914-820A>T	XP_011536567.1:n.2914-820A>T
XM_017019252.2:c.2308-820A>T	XP_016874741.1:n.2308-820A>T
XR_002957320.1:n.3672-820A>T
XR_002957321.1:n.3672-820A>T
XR_002957322.1:n.2559-820A>T
XR_944530.2:n.3672-820A>T
XR_944532.3:n.3672-820A>T
NM_001093.4:c.2914-820A>T MANE Select	NP_001084.3:n.2914-820A>T