Canonical Allele Identifier: CA1917101426
Gene: SIRT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67917000A= , CM000672.2:g.67917000A= GRCh38
NC_000010.10:g.69676757A= , CM000672.1:g.69676757A= GRCh37
NC_000010.9:g.69346763A= NCBI36
NG_050664.1:g.37339A=

Transcript Alleles

HGVS Amino-acid change
ENST00000212015.11:c.*407A= MANE Select ENSP00000212015.6:n.*407A=
ENST00000212015.10:c.*407A= ENSP00000212015.6:n.*407A=
ENST00000403579.1:c.*407A= ENSP00000384063.1:n.*407A=
ENST00000406900.5:c.*407A= ENSP00000384508.1:n.*407A=
ENST00000432464.5:c.*407A= ENSP00000409208.1:n.*407A=
NM_001142498.1:c.*407A= NP_001135970.1:n.*407A=
NM_001314049.1:c.*407A= NP_001300978.1:n.*407A=
NM_012238.4:c.*407A= NP_036370.2:n.*407A=
XM_006717737.2:c.*407A= XP_006717800.1:n.*407A=
XM_011539561.1:c.*407A= XP_011537863.1:n.*407A=
NM_012238.5:c.*407A= MANE Select NP_036370.2:n.*407A=
NM_001142498.2:c.*407A= NP_001135970.1:n.*407A=