Canonical Allele Identifier: CA891836510

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961044_87961045delinsTG , CM000672.2:g.87961044_87961045delinsTG	GRCh38
NC_000010.10:g.89720801_89720802delinsTG , CM000672.1:g.89720801_89720802delinsTG	GRCh37
NC_000010.9:g.89710781_89710782delinsTG	NCBI36
NG_007466.2:g.102606_102607delinsTG , LRG_311:g.102606_102607delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1045_1046delinsTG	ENSP00000514759.2:p.Leu349Cys
ENST00000710265.1:c.952_953delinsTG	ENSP00000518161.1:p.Leu318Cys
ENST00000472832.3:c.952_953delinsTG	ENSP00000483066.2:p.Leu318Cys
ENST00000688158.2:n.1687_1688delinsTG
ENST00000688922.2:c.*782_*783delinsTG	ENSP00000508742.2:n.*782_*783delinsTG
ENST00000700021.1:c.907_908delinsTG	ENSP00000514757.1:p.Leu303Cys
ENST00000700022.1:c.*291_*292delinsTG	ENSP00000514758.1:n.*291_*292delinsTG
ENST00000700023.1:n.2110_2111delinsTG
ENST00000700024.1:n.2344_2345delinsTG
ENST00000700025.1:n.1721_1722delinsTG
ENST00000700026.1:n.589_590delinsTG
ENST00000706954.1:c.952_953delinsTG	ENSP00000516674.1:p.Leu318Cys
ENST00000706955.1:c.*987_*988delinsTG	ENSP00000516675.1:n.*987_*988delinsTG
ENST00000686459.1:c.*538_*539delinsTG	ENSP00000508909.1:n.*538_*539delinsTG
ENST00000688158.1:c.*1063_*1064delinsTG	ENSP00000509254.1:n.*1063_*1064delinsTG
ENST00000688308.1:c.952_953delinsTG	ENSP00000508752.1:p.Leu318Cys
ENST00000688922.1:c.873_874delinsTG
ENST00000693560.1:c.1471_1472delinsTG	ENSP00000509861.1:p.Leu491Cys
ENST00000371953.8:c.952_953delinsTG MANE Select	ENSP00000361021.3:p.Leu318Cys
ENST00000371953.7:c.952_953delinsTG	ENSP00000361021.3:p.Leu318Cys
ENST00000472832.2:c.379_380delinsTG	ENSP00000483066.1:p.Leu127Cys
NM_000314.5:c.952_953delinsTG	NP_000305.3:p.Leu318Cys
NM_000314.6:c.952_953delinsTG	NP_000305.3:p.Leu318Cys
NM_001304717.2:c.1471_1472delinsTG	NP_001291646.2:p.Leu491Cys
NM_001304718.1:c.361_362delinsTG	NP_001291647.1:p.Leu121Cys
XM_006717926.2:c.907_908delinsTG	XP_006717989.1:p.Leu303Cys
XM_011539981.1:c.952_953delinsTG	XP_011538283.1:p.Leu318Cys
XM_011539982.1:c.856_857delinsTG	XP_011538284.1:p.Leu286Cys
XR_945791.1:n.1522_1523delinsTG
NM_000314.7:c.952_953delinsTG	NP_000305.3:p.Leu318Cys
NM_001304717.5:c.1471_1472delinsTG	NP_001291646.4:p.Leu491Cys
NM_001304718.2:c.361_362delinsTG	NP_001291647.1:p.Leu121Cys
NM_000314.8:c.952_953delinsTG MANE Select	NP_000305.3:p.Leu318Cys