Canonical Allele Identifier: CA338319

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933196T>G , CM000672.2:g.87933196T>G	GRCh38
NC_000010.10:g.89692953T>G , CM000672.1:g.89692953T>G	GRCh37
NC_000010.9:g.89682933T>G	NCBI36
NG_007466.2:g.74758T>G , LRG_311:g.74758T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000314.8:c.437T>G MANE Select	NP_000305.3:p.Leu146Ter
ENST00000371953.8:c.437T>G MANE Select	ENSP00000361021.3:p.Leu146Ter
NM_000314.5:c.437T>G	NP_000305.3:p.Leu146Ter
NM_000314.6:c.437T>G	NP_000305.3:p.Leu146Ter
NM_000314.7:c.437T>G	NP_000305.3:p.Leu146Ter
NM_001304717.2:c.956T>G	NP_001291646.2:p.Leu319Ter
NM_001304717.5:c.956T>G	NP_001291646.4:p.Leu319Ter
NM_001304718.1:c.-314T>G	NP_001291647.1:n.-314T>G
NM_001304718.2:c.-314T>G	NP_001291647.1:n.-314T>G
ENST00000371953.7:c.437T>G	ENSP00000361021.3:p.Leu146Ter
ENST00000472832.3:c.437T>G	ENSP00000483066.2:p.Leu146Ter
ENST00000498703.1:n.263T>G
ENST00000610634.1:c.335T>G	ENSP00000477517.1:p.Leu112Ter
ENST00000686459.1:c.437T>G	ENSP00000508909.1:p.Leu146Ter
ENST00000688158.1:c.*548T>G	ENSP00000509254.1:n.*548T>G
ENST00000688158.2:n.1172T>G
ENST00000688308.1:c.437T>G	ENSP00000508752.1:p.Leu146Ter
ENST00000688922.1:c.358T>G
ENST00000688922.2:c.*267T>G	ENSP00000508742.2:n.*267T>G
ENST00000693560.1:c.956T>G	ENSP00000509861.1:p.Leu319Ter
ENST00000700021.1:c.392T>G	ENSP00000514757.1:p.Leu131Ter
ENST00000700022.1:c.437T>G	ENSP00000514758.1:p.Leu146Ter
ENST00000700029.1:c.271T>G
ENST00000700029.2:c.437T>G	ENSP00000514759.2:p.Leu146Ter
ENST00000706954.1:c.437T>G	ENSP00000516674.1:p.Leu146Ter
ENST00000706955.1:c.*472T>G	ENSP00000516675.1:n.*472T>G
ENST00000710265.1:c.437T>G	ENSP00000518161.1:p.Leu146Ter
XM_006717926.2:c.392T>G	XP_006717989.1:p.Leu131Ter
XM_011539981.1:c.437T>G	XP_011538283.1:p.Leu146Ter
XM_011539982.1:c.341T>G	XP_011538284.1:p.Leu114Ter
XR_945789.1:n.1149T>G
XR_945790.1:n.1149T>G
XR_945791.1:n.1149T>G