Canonical Allele Identifier: CA891835438

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894093_87894094delinsTC , CM000672.2:g.87894093_87894094delinsTC	GRCh38
NC_000010.10:g.89653850_89653851delinsTC , CM000672.1:g.89653850_89653851delinsTC	GRCh37
NC_000010.9:g.89643830_89643831delinsTC	NCBI36
NG_007466.2:g.35655_35656delinsTC , LRG_311:g.35655_35656delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.148_149delinsTC	ENSP00000514759.2:p.Ile50Ser
ENST00000710265.1:c.148_149delinsTC	ENSP00000518161.1:p.Ile50Ser
ENST00000472832.3:c.148_149delinsTC	ENSP00000483066.2:p.Ile50Ser
ENST00000688158.2:n.899+13655_899+13656delinsTC
ENST00000688922.2:c.148_149delinsTC	ENSP00000508742.2:p.Ile50Ser
ENST00000700021.1:c.148_149delinsTC	ENSP00000514757.1:p.Ile50Ser
ENST00000700022.1:c.148_149delinsTC	ENSP00000514758.1:p.Ile50Ser
ENST00000706954.1:c.148_149delinsTC	ENSP00000516674.1:p.Ile50Ser
ENST00000706955.1:c.*183_*184delinsTC	ENSP00000516675.1:n.*183_*184delinsTC
ENST00000686459.1:c.148_149delinsTC	ENSP00000508909.1:p.Ile50Ser
ENST00000688158.1:c.*275+13655_*275+13656delinsTC	ENSP00000509254.1:n.*275+13655_*275+13656delinsTC
ENST00000688308.1:c.148_149delinsTC	ENSP00000508752.1:p.Ile50Ser
ENST00000688922.1:c.17_18delinsTC
ENST00000693560.1:c.667_668delinsTC	ENSP00000509861.1:p.Ile223Ser
ENST00000371953.8:c.148_149delinsTC MANE Select	ENSP00000361021.3:p.Ile50Ser
ENST00000371953.7:c.148_149delinsTC	ENSP00000361021.3:p.Ile50Ser
ENST00000462694.1:n.150_151delinsTC
ENST00000610634.1:c.46_47delinsTC	ENSP00000477517.1:p.Ile16Ser
NM_000314.5:c.148_149delinsTC	NP_000305.3:p.Ile50Ser
NM_000314.6:c.148_149delinsTC	NP_000305.3:p.Ile50Ser
NM_001304717.2:c.667_668delinsTC	NP_001291646.2:p.Ile223Ser
NM_001304718.1:c.-558_-557delinsTC	NP_001291647.1:n.-558_-557delinsTC
XM_006717926.2:c.148_149delinsTC	XP_006717989.1:p.Ile50Ser
XM_011539981.1:c.148_149delinsTC	XP_011538283.1:p.Ile50Ser
XM_011539982.1:c.68+13655_68+13656delinsTC	XP_011538284.1:n.68+13655_68+13656delinsTC
XR_945789.1:n.860_861delinsTC
XR_945790.1:n.860_861delinsTC
XR_945791.1:n.860_861delinsTC
NM_000314.7:c.148_149delinsTC	NP_000305.3:p.Ile50Ser
NM_001304717.5:c.667_668delinsTC	NP_001291646.4:p.Ile223Ser
NM_001304718.2:c.-558_-557delinsTC	NP_001291647.1:n.-558_-557delinsTC
NM_000314.8:c.148_149delinsTC MANE Select	NP_000305.3:p.Ile50Ser