Canonical Allele Identifier: CA1148219389

Gene: HMGCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119759714C= , CM000663.2:g.119759714C=	GRCh38
NC_000001.10:g.120302337C= , CM000663.1:g.120302337C=	GRCh37
NC_000001.9:g.120103860C=	NCBI36
NG_013348.1:g.14219G= , LRG_447:g.14219G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369406.8:c.685+150G= MANE Select	ENSP00000358414.3:n.685+150G=
ENST00000369406.7:c.685+150G=	ENSP00000358414.3:n.685+150G=
ENST00000476640.1:n.581+150G=
ENST00000544913.2:c.560-432G=	ENSP00000439495.2:n.560-432G=
NM_001166107.1:c.560-432G= , LRG_447t2:c.560-432G=	NP_001159579.1:n.560-432G=
NM_005518.3:c.685+150G= , LRG_447t1:c.685+150G=	NP_005509.1:n.685+150G=
XM_011541313.1:c.685+150G=	XP_011539615.1:n.685+150G=
XM_011541313.2:c.685+150G=	XP_011539615.1:n.685+150G=
NM_005518.4:c.685+150G= MANE Select	NP_005509.1:n.685+150G=