Canonical Allele Identifier: CA891836814

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933067_87933068delinsAT , CM000672.2:g.87933067_87933068delinsAT	GRCh38
NC_000010.10:g.89692824_89692825delinsAT , CM000672.1:g.89692824_89692825delinsAT	GRCh37
NC_000010.9:g.89682804_89682805delinsAT	NCBI36
NG_007466.2:g.74629_74630delinsAT , LRG_311:g.74629_74630delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.308_309delinsAT	ENSP00000514759.2:p.Pro103His
ENST00000710265.1:c.308_309delinsAT	ENSP00000518161.1:p.Pro103His
ENST00000472832.3:c.308_309delinsAT	ENSP00000483066.2:p.Pro103His
ENST00000688158.2:n.1043_1044delinsAT
ENST00000688922.2:c.*138_*139delinsAT	ENSP00000508742.2:n.*138_*139delinsAT
ENST00000700021.1:c.263_264delinsAT	ENSP00000514757.1:p.Pro88His
ENST00000700022.1:c.308_309delinsAT	ENSP00000514758.1:p.Pro103His
ENST00000700029.1:c.142_143delinsAT
ENST00000706954.1:c.308_309delinsAT	ENSP00000516674.1:p.Pro103His
ENST00000706955.1:c.*343_*344delinsAT	ENSP00000516675.1:n.*343_*344delinsAT
ENST00000686459.1:c.308_309delinsAT	ENSP00000508909.1:p.Pro103His
ENST00000688158.1:c.*419_*420delinsAT	ENSP00000509254.1:n.*419_*420delinsAT
ENST00000688308.1:c.308_309delinsAT	ENSP00000508752.1:p.Pro103His
ENST00000688922.1:c.229_230delinsAT
ENST00000693560.1:c.827_828delinsAT	ENSP00000509861.1:p.Pro276His
ENST00000371953.8:c.308_309delinsAT MANE Select	ENSP00000361021.3:p.Pro103His
ENST00000371953.7:c.308_309delinsAT	ENSP00000361021.3:p.Pro103His
ENST00000498703.1:n.134_135delinsAT
ENST00000610634.1:c.206_207delinsAT	ENSP00000477517.1:p.Pro69His
NM_000314.5:c.308_309delinsAT	NP_000305.3:p.Pro103His
NM_000314.6:c.308_309delinsAT	NP_000305.3:p.Pro103His
NM_001304717.2:c.827_828delinsAT	NP_001291646.2:p.Pro276His
NM_001304718.1:c.-443_-442delinsAT	NP_001291647.1:n.-443_-442delinsAT
XM_006717926.2:c.263_264delinsAT	XP_006717989.1:p.Pro88His
XM_011539981.1:c.308_309delinsAT	XP_011538283.1:p.Pro103His
XM_011539982.1:c.212_213delinsAT	XP_011538284.1:p.Pro71His
XR_945789.1:n.1020_1021delinsAT
XR_945790.1:n.1020_1021delinsAT
XR_945791.1:n.1020_1021delinsAT
NM_000314.7:c.308_309delinsAT	NP_000305.3:p.Pro103His
NM_001304717.5:c.827_828delinsAT	NP_001291646.4:p.Pro276His
NM_001304718.2:c.-443_-442delinsAT	NP_001291647.1:n.-443_-442delinsAT
NM_000314.8:c.308_309delinsAT MANE Select	NP_000305.3:p.Pro103His