Canonical Allele Identifier: CA341864330

Gene: HMGCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119764219G>A , CM000663.2:g.119764219G>A	GRCh38
NC_000001.10:g.120306842G>A , CM000663.1:g.120306842G>A	GRCh37
NC_000001.9:g.120108365G>A	NCBI36
NG_013348.1:g.9714C>T , LRG_447:g.9714C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005518.4:c.512C>T MANE Select	NP_005509.1:p.Ala171Val
ENST00000369406.8:c.512C>T MANE Select	ENSP00000358414.3:p.Ala171Val
NM_001166107.1:c.512C>T , LRG_447t2:c.512C>T	NP_001159579.1:p.Ala171Val
NM_005518.3:c.512C>T , LRG_447t1:c.512C>T	NP_005509.1:p.Ala171Val
ENST00000369406.7:c.512C>T	ENSP00000358414.3:p.Ala171Val
ENST00000476640.1:n.408C>T
ENST00000544913.2:c.512C>T	ENSP00000439495.2:p.Ala171Val
XM_011541313.1:c.512C>T	XP_011539615.1:p.Ala171Val
XM_011541313.2:c.512C>T	XP_011539615.1:p.Ala171Val