Canonical Allele Identifier: CA1917096903

Gene: SIRT1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67908156_67908157delinsTC , CM000672.2:g.67908156_67908157delinsTC	GRCh38
NC_000010.10:g.69667913_69667914delinsTC , CM000672.1:g.69667913_69667914delinsTC	GRCh37
NC_000010.9:g.69337919_69337920delinsTC	NCBI36
NG_050664.1:g.28495_28496delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.1170+31_1170+32delinsTC MANE Select	ENSP00000212015.6:n.1170+31_1170+32delinsTC
ENST00000212015.10:c.1170+31_1170+32delinsTC	ENSP00000212015.6:n.1170+31_1170+32delinsTC
ENST00000403579.1:c.261+31_261+32delinsTC	ENSP00000384063.1:n.261+31_261+32delinsTC
ENST00000406900.5:c.261+31_261+32delinsTC	ENSP00000384508.1:n.261+31_261+32delinsTC
ENST00000432464.5:c.285+31_285+32delinsTC	ENSP00000409208.1:n.285+31_285+32delinsTC
NM_001142498.1:c.285+31_285+32delinsTC	NP_001135970.1:n.285+31_285+32delinsTC
NM_001314049.1:c.261+31_261+32delinsTC	NP_001300978.1:n.261+31_261+32delinsTC
NM_012238.4:c.1170+31_1170+32delinsTC	NP_036370.2:n.1170+31_1170+32delinsTC
XM_006717737.2:c.1017+31_1017+32delinsTC	XP_006717800.1:n.1017+31_1017+32delinsTC
XM_011539561.1:c.594+31_594+32delinsTC	XP_011537863.1:n.594+31_594+32delinsTC
NM_012238.5:c.1170+31_1170+32delinsTC MANE Select	NP_036370.2:n.1170+31_1170+32delinsTC
NM_001142498.2:c.285+31_285+32delinsTC	NP_001135970.1:n.285+31_285+32delinsTC