Canonical Allele Identifier: CA341860680

Gene: HMGCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119757384G>A , CM000663.2:g.119757384G>A	GRCh38
NC_000001.10:g.120300007G>A , CM000663.1:g.120300007G>A	GRCh37
NC_000001.9:g.120101530G>A	NCBI36
NG_013348.1:g.16549C>T , LRG_447:g.16549C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005518.4:c.905C>T MANE Select	NP_005509.1:p.Thr302Ile
ENST00000369406.8:c.905C>T MANE Select	ENSP00000358414.3:p.Thr302Ile
NM_001166107.1:c.779C>T , LRG_447t2:c.779C>T	NP_001159579.1:p.Thr260Ile
NM_005518.3:c.905C>T , LRG_447t1:c.905C>T	NP_005509.1:p.Thr302Ile
ENST00000369406.7:c.905C>T	ENSP00000358414.3:p.Thr302Ile
ENST00000472375.5:n.352C>T
ENST00000476640.1:n.636C>T
ENST00000544913.2:c.779C>T	ENSP00000439495.2:p.Thr260Ile
XM_011541313.1:c.740C>T	XP_011539615.1:p.Thr247Ile
XM_011541313.2:c.740C>T	XP_011539615.1:p.Thr247Ile