Canonical Allele Identifier: CA1926182501

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952145T= , CM000672.2:g.87952145T=	GRCh38
NC_000010.10:g.89711902T= , CM000672.1:g.89711902T=	GRCh37
NC_000010.9:g.89701882T=	NCBI36
NG_007466.2:g.93707T= , LRG_311:g.93707T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000314.8:c.520T= MANE Select	NP_000305.3:p.Tyr174=
ENST00000371953.8:c.520T= MANE Select	ENSP00000361021.3:p.Tyr174=
NM_000314.5:c.520T=	NP_000305.3:p.Tyr174=
NM_000314.6:c.520T=	NP_000305.3:p.Tyr174=
NM_000314.7:c.520T=	NP_000305.3:p.Tyr174=
NM_001304717.2:c.1039T=	NP_001291646.2:p.Tyr347=
NM_001304717.5:c.1039T=	NP_001291646.4:p.Tyr347=
NM_001304718.1:c.-72T=	NP_001291647.1:n.-72T=
NM_001304718.2:c.-72T=	NP_001291647.1:n.-72T=
ENST00000371953.7:c.520T=	ENSP00000361021.3:p.Tyr174=
ENST00000472832.3:c.520T=	ENSP00000483066.2:p.Tyr174=
ENST00000686459.1:c.*106T=	ENSP00000508909.1:n.*106T=
ENST00000688158.1:c.*631T=	ENSP00000509254.1:n.*631T=
ENST00000688158.2:n.1255T=
ENST00000688308.1:c.520T=	ENSP00000508752.1:p.Tyr174=
ENST00000688922.1:c.441T=
ENST00000688922.2:c.*350T=	ENSP00000508742.2:n.*350T=
ENST00000693560.1:c.1039T=	ENSP00000509861.1:p.Tyr347=
ENST00000700021.1:c.475T=	ENSP00000514757.1:p.Tyr159=
ENST00000700022.1:c.493-5708T=	ENSP00000514758.1:n.493-5708T=
ENST00000700023.1:n.1678T=
ENST00000700024.1:n.1912T=
ENST00000700025.1:n.1289T=
ENST00000700029.1:c.354T=
ENST00000700029.2:c.520T=	ENSP00000514759.2:p.Tyr174=
ENST00000706954.1:c.520T=	ENSP00000516674.1:p.Tyr174=
ENST00000706955.1:c.*555T=	ENSP00000516675.1:n.*555T=
ENST00000710265.1:c.520T=	ENSP00000518161.1:p.Tyr174=
XM_006717926.2:c.475T=	XP_006717989.1:p.Tyr159=
XM_011539981.1:c.520T=	XP_011538283.1:p.Tyr174=
XM_011539982.1:c.424T=	XP_011538284.1:p.Tyr142=
XR_945789.1:n.1391T=
XR_945790.1:n.1508T=
XR_945791.1:n.1205-5708T=