Canonical Allele Identifier: CA2319265296

Gene: SIRT6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4176088T= , CM000681.2:g.4176088T=	GRCh38
NC_000019.9:g.4176085T= , CM000681.1:g.4176085T=	GRCh37
NC_000019.8:g.4127085T=	NCBI36
NG_047153.1:g.11512A=

Transcript Alleles

HGVS	Amino-acid Change
NM_016539.4:c.438-151A= MANE Select	NP_057623.2:n.438-151A=
ENST00000337491.7:c.438-151A= MANE Select	ENSP00000337332.1:n.438-151A=
NM_001193285.1:c.438-151A=	NP_001180214.1:n.438-151A=
NM_001193285.2:c.438-151A=	NP_001180214.1:n.438-151A=
NM_001193285.3:c.438-151A=	NP_001180214.1:n.438-151A=
NM_001321058.1:c.222-151A=	NP_001307987.1:n.222-151A=
NM_001321058.2:c.222-151A=	NP_001307987.1:n.222-151A=
NM_001321059.1:c.255-151A=	NP_001307988.1:n.255-151A=
NM_001321059.2:c.255-151A=	NP_001307988.1:n.255-151A=
NM_001321060.1:c.438-151A=	NP_001307989.1:n.438-151A=
NM_001321060.2:c.438-151A=	NP_001307989.1:n.438-151A=
NM_001321061.1:c.222-151A=	NP_001307990.1:n.222-151A=
NM_001321061.2:c.222-151A=	NP_001307990.1:n.222-151A=
NM_001321062.1:c.33-151A=	NP_001307991.1:n.33-151A=
NM_001321062.2:c.33-151A=	NP_001307991.1:n.33-151A=
NM_001321063.1:c.255-151A=	NP_001307992.1:n.255-151A=
NM_001321063.2:c.255-151A=	NP_001307992.1:n.255-151A=
NM_001321064.1:c.222-151A=	NP_001307993.1:n.222-151A=
NM_001321064.2:c.222-151A=	NP_001307993.1:n.222-151A=
NM_016539.2:c.438-151A=	NP_057623.2:n.438-151A=
NM_016539.3:c.438-151A=	NP_057623.2:n.438-151A=
ENST00000305232.10:c.438-151A=	ENSP00000305310.5:n.438-151A=
ENST00000337491.6:c.438-151A=	ENSP00000337332.1:n.438-151A=
ENST00000594279.5:c.222-151A=	ENSP00000472023.1:n.222-151A=
ENST00000595670.5:n.433-151A=
ENST00000596119.5:n.301-151A=
ENST00000596298.5:n.433-151A=
ENST00000597896.5:c.216-151A=	ENSP00000470215.1:n.216-151A=
ENST00000599365.5:c.*178-151A=	ENSP00000473085.1:n.*178-151A=
ENST00000599394.1:n.461-151A=
ENST00000600540.5:n.336-151A=
ENST00000600938.5:c.*178-151A=	ENSP00000471123.1:n.*178-151A=
ENST00000601069.5:n.282-151A=
ENST00000601488.5:c.255-151A=	ENSP00000469001.1:n.255-151A=
ENST00000601571.1:c.249-151A=	ENSP00000471837.1:n.249-151A=
XM_005259574.1:c.255-151A=	XP_005259631.1:n.255-151A=
XM_005259575.1:c.222-151A=	XP_005259632.1:n.222-151A=
XM_005259577.3:c.438-151A=	XP_005259634.1:n.438-151A=
XM_024451539.1:c.366-151A=	XP_024307307.1:n.366-151A=
XM_024451540.1:c.222-151A=	XP_024307308.1:n.222-151A=