Canonical Allele Identifier: CA2609362397

Gene: SIRT1

Linked Data

• gnomAD v4: 10-67917150-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67917150G>T , CM000672.2:g.67917150G>T	GRCh38
NC_000010.10:g.69676907G>T , CM000672.1:g.69676907G>T	GRCh37
NC_000010.9:g.69346913G>T	NCBI36
NG_050664.1:g.37489G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000212015.11:c.*557G>T MANE Select	ENSP00000212015.6:n.*557G>T
ENST00000212015.10:c.*557G>T	ENSP00000212015.6:n.*557G>T
ENST00000403579.1:c.*557G>T	ENSP00000384063.1:n.*557G>T
ENST00000406900.5:c.*557G>T	ENSP00000384508.1:n.*557G>T
ENST00000432464.5:c.*557G>T	ENSP00000409208.1:n.*557G>T
NM_001142498.1:c.*557G>T	NP_001135970.1:n.*557G>T
NM_001314049.1:c.*557G>T	NP_001300978.1:n.*557G>T
NM_012238.4:c.*557G>T	NP_036370.2:n.*557G>T
XM_006717737.2:c.*557G>T	XP_006717800.1:n.*557G>T
XM_011539561.1:c.*557G>T	XP_011537863.1:n.*557G>T
NM_012238.5:c.*557G>T MANE Select	NP_036370.2:n.*557G>T
NM_001142498.2:c.*557G>T	NP_001135970.1:n.*557G>T