Canonical Allele Identifier: CA6772883

Gene: ACACB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109139539A>G , CM000674.2:g.109139539A>G	GRCh38
NC_000012.11:g.109577344A>G , CM000674.1:g.109577344A>G	GRCh37
NC_000012.10:g.108061727A>G	NCBI36
NG_046907.1:g.33356A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001093.4:c.134A>G MANE Select	NP_001084.3:p.Gln45Arg
ENST00000338432.12:c.134A>G MANE Select	ENSP00000341044.7:p.Gln45Arg
NM_001093.3:c.134A>G	NP_001084.3:p.Gln45Arg
ENST00000338432.11:c.134A>G	ENSP00000341044.7:p.Gln45Arg
ENST00000377848.7:c.134A>G	ENSP00000367079.3:p.Gln45Arg
ENST00000377854.9:c.-3869A>G	ENSP00000367085.6:n.-3869A>G
ENST00000539864.1:c.59A>G	ENSP00000443494.1:p.Gln20Arg
XM_005253876.3:c.134A>G	XP_005253933.1:p.Gln45Arg
XM_005253876.4:c.134A>G	XP_005253933.1:p.Gln45Arg
XM_006719365.2:c.134A>G	XP_006719428.1:p.Gln45Arg
XM_011538259.1:c.134A>G	XP_011536561.1:p.Gln45Arg
XM_011538259.2:c.134A>G	XP_011536561.1:p.Gln45Arg
XM_011538260.1:c.134A>G	XP_011536562.1:p.Gln45Arg
XM_011538261.1:c.134A>G	XP_011536563.1:p.Gln45Arg
XM_011538262.1:c.134A>G	XP_011536564.1:p.Gln45Arg
XM_011538263.1:c.134A>G	XP_011536565.1:p.Gln45Arg
XM_011538263.3:c.134A>G	XP_011536565.1:p.Gln45Arg
XM_011538264.1:c.26+26124A>G	XP_011536566.1:n.26+26124A>G
XM_011538264.3:c.26+26124A>G	XP_011536566.1:n.26+26124A>G
XM_011538265.1:c.134A>G	XP_011536567.1:p.Gln45Arg
XM_011538265.2:c.134A>G	XP_011536567.1:p.Gln45Arg
XR_002957320.1:n.892A>G
XR_002957321.1:n.892A>G
XR_944530.1:n.881A>G
XR_944530.2:n.892A>G
XR_944531.1:n.881A>G
XR_944532.1:n.881A>G
XR_944532.3:n.892A>G
XR_944533.1:n.882A>G