Canonical Allele Identifier: CA891834620

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894045_87894047delinsTAA , CM000672.2:g.87894045_87894047delinsTAA	GRCh38
NC_000010.10:g.89653802_89653804delinsTAA , CM000672.1:g.89653802_89653804delinsTAA	GRCh37
NC_000010.9:g.89643782_89643784delinsTAA	NCBI36
NG_007466.2:g.35607_35609delinsTAA , LRG_311:g.35607_35609delinsTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.100_102delinsTAA	ENSP00000514759.2:p.Ala34Ter
ENST00000710265.1:c.100_102delinsTAA	ENSP00000518161.1:p.Ala34Ter
ENST00000472832.3:c.100_102delinsTAA	ENSP00000483066.2:p.Ala34Ter
ENST00000688158.2:n.899+13607_899+13609delinsTAA
ENST00000688922.2:c.100_102delinsTAA	ENSP00000508742.2:p.Ala34Ter
ENST00000700021.1:c.100_102delinsTAA	ENSP00000514757.1:p.Ala34Ter
ENST00000700022.1:c.100_102delinsTAA	ENSP00000514758.1:p.Ala34Ter
ENST00000706954.1:c.100_102delinsTAA	ENSP00000516674.1:p.Ala34Ter
ENST00000706955.1:c.*135_*137delinsTAA	ENSP00000516675.1:n.*135_*137delinsTAA
ENST00000686459.1:c.100_102delinsTAA	ENSP00000508909.1:p.Ala34Ter
ENST00000688158.1:c.*275+13607_*275+13609delinsTAA	ENSP00000509254.1:n.*275+13607_*275+13609delinsTAA
ENST00000688308.1:c.100_102delinsTAA	ENSP00000508752.1:p.Ala34Ter
ENST00000693560.1:c.619_621delinsTAA	ENSP00000509861.1:p.Ala207Ter
ENST00000371953.8:c.100_102delinsTAA MANE Select	ENSP00000361021.3:p.Ala34Ter
ENST00000371953.7:c.100_102delinsTAA	ENSP00000361021.3:p.Ala34Ter
ENST00000462694.1:n.102_104delinsTAA
ENST00000610634.1:c.-3_-1delinsTAA	ENSP00000477517.1:n.-3_-1delinsTAA
NM_000314.5:c.100_102delinsTAA	NP_000305.3:p.Ala34Ter
NM_000314.6:c.100_102delinsTAA	NP_000305.3:p.Ala34Ter
NM_001304717.2:c.619_621delinsTAA	NP_001291646.2:p.Ala207Ter
NM_001304718.1:c.-606_-604delinsTAA	NP_001291647.1:n.-606_-604delinsTAA
XM_006717926.2:c.100_102delinsTAA	XP_006717989.1:p.Ala34Ter
XM_011539981.1:c.100_102delinsTAA	XP_011538283.1:p.Ala34Ter
XM_011539982.1:c.68+13607_68+13609delinsTAA	XP_011538284.1:n.68+13607_68+13609delinsTAA
XR_945789.1:n.812_814delinsTAA
XR_945790.1:n.812_814delinsTAA
XR_945791.1:n.812_814delinsTAA
NM_000314.7:c.100_102delinsTAA	NP_000305.3:p.Ala34Ter
NM_001304717.5:c.619_621delinsTAA	NP_001291646.4:p.Ala207Ter
NM_001304718.2:c.-606_-604delinsTAA	NP_001291647.1:n.-606_-604delinsTAA
NM_000314.8:c.100_102delinsTAA MANE Select	NP_000305.3:p.Ala34Ter