Canonical Allele Identifier: CA341857923
Gene: HMGCS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119753290A>C , CM000663.2:g.119753290A>C GRCh38
NC_000001.10:g.120295913A>C , CM000663.1:g.120295913A>C GRCh37
NC_000001.9:g.120097436A>C NCBI36
NG_013348.1:g.20643T>G , LRG_447:g.20643T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369406.8:c.1284T>G MANE Select ENSP00000358414.3:p.Asp428Glu
ENST00000369406.7:c.1284T>G ENSP00000358414.3:p.Asp428Glu
ENST00000544913.2:c.1158T>G ENSP00000439495.2:p.Asp386Glu
NM_001166107.1:c.1158T>G , LRG_447t2:c.1158T>G NP_001159579.1:p.Asp386Glu
NM_005518.3:c.1284T>G , LRG_447t1:c.1284T>G NP_005509.1:p.Asp428Glu
XM_011541313.1:c.1119T>G XP_011539615.1:p.Asp373Glu
XM_011541313.2:c.1119T>G XP_011539615.1:p.Asp373Glu
NM_005518.4:c.1284T>G MANE Select NP_005509.1:p.Asp428Glu