Canonical Allele Identifier: CA1917088633

Gene: SIRT1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67888811T= , CM000672.2:g.67888811T=	GRCh38
NC_000010.10:g.69648569T= , CM000672.1:g.69648569T=	GRCh37
NC_000010.9:g.69318575T=	NCBI36
NG_050664.1:g.9150T=

Transcript Alleles

HGVS	Amino-acid Change
NM_012238.5:c.548-71T= MANE Select	NP_036370.2:n.548-71T=
ENST00000212015.11:c.548-71T= MANE Select	ENSP00000212015.6:n.548-71T=
NM_001142498.1:c.-97+1278T=	NP_001135970.1:n.-97+1278T=
NM_001142498.2:c.-97+1278T=	NP_001135970.1:n.-97+1278T=
NM_012238.4:c.548-71T=	NP_036370.2:n.548-71T=
ENST00000212015.10:c.548-71T=	ENSP00000212015.6:n.548-71T=
ENST00000432464.5:c.-97+1278T=	ENSP00000409208.1:n.-97+1278T=
ENST00000473922.1:n.333+1278T=
ENST00000497639.5:n.337-71T=
XM_006717737.2:c.548-71T=	XP_006717800.1:n.548-71T=
XM_011539561.1:c.-29-71T=	XP_011537863.1:n.-29-71T=