Canonical Allele Identifier: CA2335252558

Gene: SIRT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38894892T= , CM000681.2:g.38894892T=	GRCh38
NC_000019.9:g.39385532T= , CM000681.1:g.39385532T=	GRCh37
NC_000019.8:g.44077372T=	NCBI36
NG_029624.1:g.193T=

Transcript Alleles

HGVS	Amino-acid Change
NM_012237.4:c.64-1025A= MANE Select	NP_036369.2:n.64-1025A=
ENST00000249396.12:c.64-1025A= MANE Select	ENSP00000249396.7:n.64-1025A=
NM_001193286.1:c.-48-1025A=	NP_001180215.1:n.-48-1025A=
NM_001193286.2:c.-48-1025A=	NP_001180215.1:n.-48-1025A=
NM_012237.3:c.64-1025A=	NP_036369.2:n.64-1025A=
NM_030593.2:c.-48-1025A=	NP_085096.1:n.-48-1025A=
NM_030593.3:c.-48-1025A=	NP_085096.1:n.-48-1025A=
ENST00000249396.11:c.64-1025A=	ENSP00000249396.7:n.64-1025A=
ENST00000358931.9:c.-48-1025A=	ENSP00000351809.6:n.-48-1025A=
ENST00000392081.6:c.-48-1025A=	ENSP00000375931.2:n.-48-1025A=
ENST00000407552.5:c.-48-1025A=	ENSP00000385146.1:n.-48-1025A=
ENST00000414941.5:c.-48-1025A=	ENSP00000404309.1:n.-48-1025A=
ENST00000420440.5:c.-48-1025A=	ENSP00000400338.1:n.-48-1025A=
ENST00000423526.5:c.-48-1025A=	ENSP00000409690.1:n.-48-1025A=
ENST00000437828.5:c.-179-894A=	ENSP00000397022.1:n.-179-894A=
ENST00000443898.5:c.64-921A=	ENSP00000411393.1:n.64-921A=
ENST00000447739.1:c.-152-921A=	ENSP00000408023.1:n.-152-921A=
ENST00000451193.5:c.-48-1025A=	ENSP00000407272.1:n.-48-1025A=
ENST00000476771.5:n.14-1025A=
ENST00000491960.5:n.96-1025A=
XM_006723111.1:c.-48-1025A=	XP_006723174.1:n.-48-1025A=
XM_011526654.1:c.-152-921A=	XP_011524956.1:n.-152-921A=
XM_011526654.2:c.-152-921A=	XP_011524956.1:n.-152-921A=
XM_011526655.1:c.16+4614A=	XP_011524957.1:n.16+4614A=
XM_011526656.1:c.64-1025A=	XP_011524958.1:n.64-1025A=
XM_017026500.1:c.-474-1025A=	XP_016881989.1:n.-474-1025A=
XR_001753638.2:n.189-1025A=
XR_001753639.2:n.143-1025A=