Canonical Allele Identifier: CA891838691

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952136_87952138delinsGAA , CM000672.2:g.87952136_87952138delinsGAA	GRCh38
NC_000010.10:g.89711893_89711895delinsGAA , CM000672.1:g.89711893_89711895delinsGAA	GRCh37
NC_000010.9:g.89701873_89701875delinsGAA	NCBI36
NG_007466.2:g.93698_93700delinsGAA , LRG_311:g.93698_93700delinsGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.511_513delinsGAA	ENSP00000514759.2:p.Gln171Glu
ENST00000710265.1:c.511_513delinsGAA	ENSP00000518161.1:p.Gln171Glu
ENST00000472832.3:c.511_513delinsGAA	ENSP00000483066.2:p.Gln171Glu
ENST00000688158.2:n.1246_1248delinsGAA
ENST00000688922.2:c.*341_*343delinsGAA	ENSP00000508742.2:n.*341_*343delinsGAA
ENST00000700021.1:c.466_468delinsGAA	ENSP00000514757.1:p.Gln156Glu
ENST00000700022.1:c.493-5717_493-5715delinsGAA	ENSP00000514758.1:n.493-5717_493-5715delinsGAA
ENST00000700023.1:n.1669_1671delinsGAA
ENST00000700024.1:n.1903_1905delinsGAA
ENST00000700025.1:n.1280_1282delinsGAA
ENST00000700029.1:c.345_347delinsGAA
ENST00000706954.1:c.511_513delinsGAA	ENSP00000516674.1:p.Gln171Glu
ENST00000706955.1:c.*546_*548delinsGAA	ENSP00000516675.1:n.*546_*548delinsGAA
ENST00000686459.1:c.*97_*99delinsGAA	ENSP00000508909.1:n.*97_*99delinsGAA
ENST00000688158.1:c.*622_*624delinsGAA	ENSP00000509254.1:n.*622_*624delinsGAA
ENST00000688308.1:c.511_513delinsGAA	ENSP00000508752.1:p.Gln171Glu
ENST00000688922.1:c.432_434delinsGAA
ENST00000693560.1:c.1030_1032delinsGAA	ENSP00000509861.1:p.Gln344Glu
ENST00000371953.8:c.511_513delinsGAA MANE Select	ENSP00000361021.3:p.Gln171Glu
ENST00000371953.7:c.511_513delinsGAA	ENSP00000361021.3:p.Gln171Glu
NM_000314.5:c.511_513delinsGAA	NP_000305.3:p.Gln171Glu
NM_000314.6:c.511_513delinsGAA	NP_000305.3:p.Gln171Glu
NM_001304717.2:c.1030_1032delinsGAA	NP_001291646.2:p.Gln344Glu
NM_001304718.1:c.-81_-79delinsGAA	NP_001291647.1:n.-81_-79delinsGAA
XM_006717926.2:c.466_468delinsGAA	XP_006717989.1:p.Gln156Glu
XM_011539981.1:c.511_513delinsGAA	XP_011538283.1:p.Gln171Glu
XM_011539982.1:c.415_417delinsGAA	XP_011538284.1:p.Gln139Glu
XR_945789.1:n.1382_1384delinsGAA
XR_945790.1:n.1499_1501delinsGAA
XR_945791.1:n.1205-5717_1205-5715delinsGAA
NM_000314.7:c.511_513delinsGAA	NP_000305.3:p.Gln171Glu
NM_001304717.5:c.1030_1032delinsGAA	NP_001291646.4:p.Gln344Glu
NM_001304718.2:c.-81_-79delinsGAA	NP_001291647.1:n.-81_-79delinsGAA
NM_000314.8:c.511_513delinsGAA MANE Select	NP_000305.3:p.Gln171Glu