Canonical Allele Identifier: CA891835371

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925556_87925557delinsTG , CM000672.2:g.87925556_87925557delinsTG	GRCh38
NC_000010.10:g.89685313_89685314delinsTG , CM000672.1:g.89685313_89685314delinsTG	GRCh37
NC_000010.9:g.89675293_89675294delinsTG	NCBI36
NG_007466.2:g.67118_67119delinsTG , LRG_311:g.67118_67119delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.208_209delinsTG	ENSP00000514759.2:p.Leu70Cys
ENST00000710265.1:c.208_209delinsTG	ENSP00000518161.1:p.Leu70Cys
ENST00000472832.3:c.208_209delinsTG	ENSP00000483066.2:p.Leu70Cys
ENST00000688158.2:n.943_944delinsTG
ENST00000688922.2:c.208_209delinsTG	ENSP00000508742.2:p.Leu70Ter
ENST00000700021.1:c.165-5490_165-5489delinsTG	ENSP00000514757.1:n.165-5490_165-5489delinsTG
ENST00000700022.1:c.208_209delinsTG	ENSP00000514758.1:p.Leu70Cys
ENST00000700029.1:c.42_43delinsTG
ENST00000706954.1:c.208_209delinsTG	ENSP00000516674.1:p.Leu70Cys
ENST00000706955.1:c.*243_*244delinsTG	ENSP00000516675.1:n.*243_*244delinsTG
ENST00000686459.1:c.208_209delinsTG	ENSP00000508909.1:p.Leu70Cys
ENST00000688158.1:c.*319_*320delinsTG	ENSP00000509254.1:n.*319_*320delinsTG
ENST00000688308.1:c.208_209delinsTG	ENSP00000508752.1:p.Leu70Cys
ENST00000688922.1:c.77_78delinsTG
ENST00000693560.1:c.727_728delinsTG	ENSP00000509861.1:p.Leu243Cys
ENST00000371953.8:c.208_209delinsTG MANE Select	ENSP00000361021.3:p.Leu70Cys
ENST00000371953.7:c.208_209delinsTG	ENSP00000361021.3:p.Leu70Cys
ENST00000498703.1:n.34_35delinsTG
ENST00000610634.1:c.106_107delinsTG	ENSP00000477517.1:p.Leu36Cys
NM_000314.5:c.208_209delinsTG	NP_000305.3:p.Leu70Cys
NM_000314.6:c.208_209delinsTG	NP_000305.3:p.Leu70Cys
NM_001304717.2:c.727_728delinsTG	NP_001291646.2:p.Leu243Cys
NM_001304718.1:c.-541-5490_-541-5489delinsTG	NP_001291647.1:n.-541-5490_-541-5489delinsTG
XM_006717926.2:c.165-5490_165-5489delinsTG	XP_006717989.1:n.165-5490_165-5489delinsTG
XM_011539981.1:c.208_209delinsTG	XP_011538283.1:p.Leu70Cys
XM_011539982.1:c.112_113delinsTG	XP_011538284.1:p.Leu38Cys
XR_945789.1:n.920_921delinsTG
XR_945790.1:n.920_921delinsTG
XR_945791.1:n.920_921delinsTG
NM_000314.7:c.208_209delinsTG	NP_000305.3:p.Leu70Cys
NM_001304717.5:c.727_728delinsTG	NP_001291646.4:p.Leu243Cys
NM_001304718.2:c.-541-5490_-541-5489delinsTG	NP_001291647.1:n.-541-5490_-541-5489delinsTG
NM_000314.8:c.208_209delinsTG MANE Select	NP_000305.3:p.Leu70Cys