Canonical Allele Identifier: CA891835747

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960993_87960995delinsTAA , CM000672.2:g.87960993_87960995delinsTAA	GRCh38
NC_000010.10:g.89720750_89720752delinsTAA , CM000672.1:g.89720750_89720752delinsTAA	GRCh37
NC_000010.9:g.89710730_89710732delinsTAA	NCBI36
NG_007466.2:g.102555_102557delinsTAA , LRG_311:g.102555_102557delinsTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.994_996delinsTAA	ENSP00000514759.2:p.Asp332Ter
ENST00000710265.1:c.901_903delinsTAA	ENSP00000518161.1:p.Asp301Ter
ENST00000472832.3:c.901_903delinsTAA	ENSP00000483066.2:p.Asp301Ter
ENST00000688158.2:n.1636_1638delinsTAA
ENST00000688922.2:c.*731_*733delinsTAA	ENSP00000508742.2:n.*731_*733delinsTAA
ENST00000700021.1:c.856_858delinsTAA	ENSP00000514757.1:p.Asp286Ter
ENST00000700022.1:c.*240_*242delinsTAA	ENSP00000514758.1:n.*240_*242delinsTAA
ENST00000700023.1:n.2059_2061delinsTAA
ENST00000700024.1:n.2293_2295delinsTAA
ENST00000700025.1:n.1670_1672delinsTAA
ENST00000700026.1:n.538_540delinsTAA
ENST00000706954.1:c.901_903delinsTAA	ENSP00000516674.1:p.Asp301Ter
ENST00000706955.1:c.*936_*938delinsTAA	ENSP00000516675.1:n.*936_*938delinsTAA
ENST00000686459.1:c.*487_*489delinsTAA	ENSP00000508909.1:n.*487_*489delinsTAA
ENST00000688158.1:c.*1012_*1014delinsTAA	ENSP00000509254.1:n.*1012_*1014delinsTAA
ENST00000688308.1:c.901_903delinsTAA	ENSP00000508752.1:p.Asp301Ter
ENST00000688922.1:c.822_824delinsTAA
ENST00000693560.1:c.1420_1422delinsTAA	ENSP00000509861.1:p.Asp474Ter
ENST00000371953.8:c.901_903delinsTAA MANE Select	ENSP00000361021.3:p.Asp301Ter
ENST00000371953.7:c.901_903delinsTAA	ENSP00000361021.3:p.Asp301Ter
ENST00000472832.2:c.328_330delinsTAA	ENSP00000483066.1:p.Asp110Ter
NM_000314.5:c.901_903delinsTAA	NP_000305.3:p.Asp301Ter
NM_000314.6:c.901_903delinsTAA	NP_000305.3:p.Asp301Ter
NM_001304717.2:c.1420_1422delinsTAA	NP_001291646.2:p.Asp474Ter
NM_001304718.1:c.310_312delinsTAA	NP_001291647.1:p.Asp104Ter
XM_006717926.2:c.856_858delinsTAA	XP_006717989.1:p.Asp286Ter
XM_011539981.1:c.901_903delinsTAA	XP_011538283.1:p.Asp301Ter
XM_011539982.1:c.805_807delinsTAA	XP_011538284.1:p.Asp269Ter
XR_945791.1:n.1471_1473delinsTAA
NM_000314.7:c.901_903delinsTAA	NP_000305.3:p.Asp301Ter
NM_001304717.5:c.1420_1422delinsTAA	NP_001291646.4:p.Asp474Ter
NM_001304718.2:c.310_312delinsTAA	NP_001291647.1:p.Asp104Ter
NM_000314.8:c.901_903delinsTAA MANE Select	NP_000305.3:p.Asp301Ter