Canonical Allele Identifier: CA1926182608

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952152A= , CM000672.2:g.87952152A=	GRCh38
NC_000010.10:g.89711909A= , CM000672.1:g.89711909A=	GRCh37
NC_000010.9:g.89701889A=	NCBI36
NG_007466.2:g.93714A= , LRG_311:g.93714A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.527A=	ENSP00000514759.2:p.Tyr176=
ENST00000710265.1:c.527A=	ENSP00000518161.1:p.Tyr176=
ENST00000472832.3:c.527A=	ENSP00000483066.2:p.Tyr176=
ENST00000688158.2:n.1262A=
ENST00000688922.2:c.*357A=	ENSP00000508742.2:n.*357A=
ENST00000700021.1:c.482A=	ENSP00000514757.1:p.Tyr161=
ENST00000700022.1:c.493-5701A=	ENSP00000514758.1:n.493-5701A=
ENST00000700023.1:n.1685A=
ENST00000700024.1:n.1919A=
ENST00000700025.1:n.1296A=
ENST00000700029.1:c.361A=
ENST00000706954.1:c.527A=	ENSP00000516674.1:p.Tyr176=
ENST00000706955.1:c.*562A=	ENSP00000516675.1:n.*562A=
ENST00000686459.1:c.*113A=	ENSP00000508909.1:n.*113A=
ENST00000688158.1:c.*638A=	ENSP00000509254.1:n.*638A=
ENST00000688308.1:c.527A=	ENSP00000508752.1:p.Tyr176=
ENST00000688922.1:c.448A=
ENST00000693560.1:c.1046A=	ENSP00000509861.1:p.Tyr349=
ENST00000371953.8:c.527A= MANE Select	ENSP00000361021.3:p.Tyr176=
ENST00000371953.7:c.527A=	ENSP00000361021.3:p.Tyr176=
NM_000314.5:c.527A=	NP_000305.3:p.Tyr176=
NM_000314.6:c.527A=	NP_000305.3:p.Tyr176=
NM_001304717.2:c.1046A=	NP_001291646.2:p.Tyr349=
NM_001304718.1:c.-65A=	NP_001291647.1:n.-65A=
XM_006717926.2:c.482A=	XP_006717989.1:p.Tyr161=
XM_011539981.1:c.527A=	XP_011538283.1:p.Tyr176=
XM_011539982.1:c.431A=	XP_011538284.1:p.Tyr144=
XR_945789.1:n.1398A=
XR_945790.1:n.1515A=
XR_945791.1:n.1205-5701A=
NM_000314.7:c.527A=	NP_000305.3:p.Tyr176=
NM_001304717.5:c.1046A=	NP_001291646.4:p.Tyr349=
NM_001304718.2:c.-65A=	NP_001291647.1:n.-65A=
NM_000314.8:c.527A= MANE Select	NP_000305.3:p.Tyr176=