Canonical Allele Identifier: CA891841524

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965296_87965297delinsCG , CM000672.2:g.87965296_87965297delinsCG	GRCh38
NC_000010.10:g.89725053_89725054delinsCG , CM000672.1:g.89725053_89725054delinsCG	GRCh37
NC_000010.9:g.89715033_89715034delinsCG	NCBI36
NG_007466.2:g.106858_106859delinsCG , LRG_311:g.106858_106859delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1129_1130delinsCG	ENSP00000514759.2:p.Tyr377Arg
ENST00000710265.1:c.*65_*66delinsCG	ENSP00000518161.1:n.*65_*66delinsCG
ENST00000688158.2:n.1771_1772delinsCG
ENST00000688922.2:c.*866_*867delinsCG	ENSP00000508742.2:n.*866_*867delinsCG
ENST00000700021.1:c.991_992delinsCG	ENSP00000514757.1:p.Tyr331Arg
ENST00000700022.1:c.*375_*376delinsCG	ENSP00000514758.1:n.*375_*376delinsCG
ENST00000700023.1:n.2194_2195delinsCG
ENST00000700024.1:n.2428_2429delinsCG
ENST00000706954.1:c.1036_1037delinsCG	ENSP00000516674.1:p.Tyr346Arg
ENST00000706955.1:c.*1071_*1072delinsCG	ENSP00000516675.1:n.*1071_*1072delinsCG
ENST00000686459.1:c.*622_*623delinsCG	ENSP00000508909.1:n.*622_*623delinsCG
ENST00000688158.1:c.*1147_*1148delinsCG	ENSP00000509254.1:n.*1147_*1148delinsCG
ENST00000688308.1:c.1036_1037delinsCG	ENSP00000508752.1:p.Tyr346Arg
ENST00000688922.1:c.957_958delinsCG
ENST00000693560.1:c.1555_1556delinsCG	ENSP00000509861.1:p.Tyr519Arg
ENST00000371953.8:c.1036_1037delinsCG MANE Select	ENSP00000361021.3:p.Tyr346Arg
ENST00000371953.7:c.1036_1037delinsCG	ENSP00000361021.3:p.Tyr346Arg
NM_000314.5:c.1036_1037delinsCG	NP_000305.3:p.Tyr346Arg
NM_000314.6:c.1036_1037delinsCG	NP_000305.3:p.Tyr346Arg
NM_001304717.2:c.1555_1556delinsCG	NP_001291646.2:p.Tyr519Arg
NM_001304718.1:c.445_446delinsCG	NP_001291647.1:p.Tyr149Arg
XM_006717926.2:c.991_992delinsCG	XP_006717989.1:p.Tyr331Arg
XM_011539982.1:c.940_941delinsCG	XP_011538284.1:p.Tyr314Arg
XR_945791.1:n.1606_1607delinsCG
NM_000314.7:c.1036_1037delinsCG	NP_000305.3:p.Tyr346Arg
NM_001304717.5:c.1555_1556delinsCG	NP_001291646.4:p.Tyr519Arg
NM_001304718.2:c.445_446delinsCG	NP_001291647.1:p.Tyr149Arg
NM_000314.8:c.1036_1037delinsCG MANE Select	NP_000305.3:p.Tyr346Arg