Canonical Allele Identifier: CA1192442491

Gene: HMGCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119759730C= , CM000663.2:g.119759730C=	GRCh38
NC_000001.10:g.120302353C= , CM000663.1:g.120302353C=	GRCh37
NC_000001.9:g.120103876C=	NCBI36
NG_013348.1:g.14203G= , LRG_447:g.14203G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369406.8:c.685+134G= MANE Select	ENSP00000358414.3:n.685+134G=
ENST00000369406.7:c.685+134G=	ENSP00000358414.3:n.685+134G=
ENST00000476640.1:n.581+134G=
ENST00000544913.2:c.560-448G=	ENSP00000439495.2:n.560-448G=
NM_001166107.1:c.560-448G= , LRG_447t2:c.560-448G=	NP_001159579.1:n.560-448G=
NM_005518.3:c.685+134G= , LRG_447t1:c.685+134G=	NP_005509.1:n.685+134G=
XM_011541313.1:c.685+134G=	XP_011539615.1:n.685+134G=
XM_011541313.2:c.685+134G=	XP_011539615.1:n.685+134G=
NM_005518.4:c.685+134G= MANE Select	NP_005509.1:n.685+134G=