Canonical Allele Identifier: CA1926175108

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933137_87933138delinsTG , CM000672.2:g.87933137_87933138delinsTG	GRCh38
NC_000010.10:g.89692894_89692895delinsTG , CM000672.1:g.89692894_89692895delinsTG	GRCh37
NC_000010.9:g.89682874_89682875delinsTG	NCBI36
NG_007466.2:g.74699_74700delinsTG , LRG_311:g.74699_74700delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.378_379delinsTG	ENSP00000514759.2:p.Ala126=
ENST00000710265.1:c.378_379delinsTG	ENSP00000518161.1:p.Ala126=
ENST00000472832.3:c.378_379delinsTG	ENSP00000483066.2:p.Ala126=
ENST00000688158.2:n.1113_1114delinsTG
ENST00000688922.2:c.*208_*209delinsTG	ENSP00000508742.2:n.*208_*209delinsTG
ENST00000700021.1:c.333_334delinsTG	ENSP00000514757.1:p.Ala111=
ENST00000700022.1:c.378_379delinsTG	ENSP00000514758.1:p.Ala126=
ENST00000700029.1:c.212_213delinsTG
ENST00000706954.1:c.378_379delinsTG	ENSP00000516674.1:p.Ala126=
ENST00000706955.1:c.*413_*414delinsTG	ENSP00000516675.1:n.*413_*414delinsTG
ENST00000686459.1:c.378_379delinsTG	ENSP00000508909.1:p.Ala126=
ENST00000688158.1:c.*489_*490delinsTG	ENSP00000509254.1:n.*489_*490delinsTG
ENST00000688308.1:c.378_379delinsTG	ENSP00000508752.1:p.Ala126=
ENST00000688922.1:c.299_300delinsTG
ENST00000693560.1:c.897_898delinsTG	ENSP00000509861.1:p.Ala299=
ENST00000371953.8:c.378_379delinsTG MANE Select	ENSP00000361021.3:p.Ala126=
ENST00000371953.7:c.378_379delinsTG	ENSP00000361021.3:p.Ala126=
ENST00000498703.1:n.204_205delinsTG
ENST00000610634.1:c.276_277delinsTG	ENSP00000477517.1:p.Ala92=
NM_000314.5:c.378_379delinsTG	NP_000305.3:p.Ala126=
NM_000314.6:c.378_379delinsTG	NP_000305.3:p.Ala126=
NM_001304717.2:c.897_898delinsTG	NP_001291646.2:p.Ala299=
NM_001304718.1:c.-373_-372delinsTG	NP_001291647.1:n.-373_-372delinsTG
XM_006717926.2:c.333_334delinsTG	XP_006717989.1:p.Ala111=
XM_011539981.1:c.378_379delinsTG	XP_011538283.1:p.Ala126=
XM_011539982.1:c.282_283delinsTG	XP_011538284.1:p.Ala94=
XR_945789.1:n.1090_1091delinsTG
XR_945790.1:n.1090_1091delinsTG
XR_945791.1:n.1090_1091delinsTG
NM_000314.7:c.378_379delinsTG	NP_000305.3:p.Ala126=
NM_001304717.5:c.897_898delinsTG	NP_001291646.4:p.Ala299=
NM_001304718.2:c.-373_-372delinsTG	NP_001291647.1:n.-373_-372delinsTG
NM_000314.8:c.378_379delinsTG MANE Select	NP_000305.3:p.Ala126=