Canonical Allele Identifier: CA1917101489

Gene: SIRT1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67917132_67917134delinsCTT , CM000672.2:g.67917132_67917134delinsCTT	GRCh38
NC_000010.10:g.69676889_69676891delinsCTT , CM000672.1:g.69676889_69676891delinsCTT	GRCh37
NC_000010.9:g.69346895_69346897delinsCTT	NCBI36
NG_050664.1:g.37471_37473delinsCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.*539_*541delinsCTT MANE Select	ENSP00000212015.6:n.*539_*541delinsCTT
ENST00000212015.10:c.*539_*541delinsCTT	ENSP00000212015.6:n.*539_*541delinsCTT
ENST00000403579.1:c.*539_*541delinsCTT	ENSP00000384063.1:n.*539_*541delinsCTT
ENST00000406900.5:c.*539_*541delinsCTT	ENSP00000384508.1:n.*539_*541delinsCTT
ENST00000432464.5:c.*539_*541delinsCTT	ENSP00000409208.1:n.*539_*541delinsCTT
NM_001142498.1:c.*539_*541delinsCTT	NP_001135970.1:n.*539_*541delinsCTT
NM_001314049.1:c.*539_*541delinsCTT	NP_001300978.1:n.*539_*541delinsCTT
NM_012238.4:c.*539_*541delinsCTT	NP_036370.2:n.*539_*541delinsCTT
XM_006717737.2:c.*539_*541delinsCTT	XP_006717800.1:n.*539_*541delinsCTT
XM_011539561.1:c.*539_*541delinsCTT	XP_011537863.1:n.*539_*541delinsCTT
NM_012238.5:c.*539_*541delinsCTT MANE Select	NP_036370.2:n.*539_*541delinsCTT
NM_001142498.2:c.*539_*541delinsCTT	NP_001135970.1:n.*539_*541delinsCTT