Canonical Allele Identifier: CA891837206

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965326_87965327delinsTG , CM000672.2:g.87965326_87965327delinsTG	GRCh38
NC_000010.10:g.89725083_89725084delinsTG , CM000672.1:g.89725083_89725084delinsTG	GRCh37
NC_000010.9:g.89715063_89715064delinsTG	NCBI36
NG_007466.2:g.106888_106889delinsTG , LRG_311:g.106888_106889delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1159_1160delinsTG	ENSP00000514759.2:p.Asn387Cys
ENST00000710265.1:c.*95_*96delinsTG	ENSP00000518161.1:n.*95_*96delinsTG
ENST00000688158.2:n.1801_1802delinsTG
ENST00000688922.2:c.*896_*897delinsTG	ENSP00000508742.2:n.*896_*897delinsTG
ENST00000700021.1:c.1021_1022delinsTG	ENSP00000514757.1:p.Asn341Cys
ENST00000700022.1:c.*405_*406delinsTG	ENSP00000514758.1:n.*405_*406delinsTG
ENST00000700023.1:n.2224_2225delinsTG
ENST00000700024.1:n.2458_2459delinsTG
ENST00000706954.1:c.1066_1067delinsTG	ENSP00000516674.1:p.Asn356Cys
ENST00000706955.1:c.*1101_*1102delinsTG	ENSP00000516675.1:n.*1101_*1102delinsTG
ENST00000686459.1:c.*652_*653delinsTG	ENSP00000508909.1:n.*652_*653delinsTG
ENST00000688158.1:c.*1177_*1178delinsTG	ENSP00000509254.1:n.*1177_*1178delinsTG
ENST00000688308.1:c.1066_1067delinsTG	ENSP00000508752.1:p.Asn356Cys
ENST00000688922.1:c.987_988delinsTG
ENST00000693560.1:c.1585_1586delinsTG	ENSP00000509861.1:p.Asn529Cys
ENST00000371953.8:c.1066_1067delinsTG MANE Select	ENSP00000361021.3:p.Asn356Cys
ENST00000371953.7:c.1066_1067delinsTG	ENSP00000361021.3:p.Asn356Cys
NM_000314.5:c.1066_1067delinsTG	NP_000305.3:p.Asn356Cys
NM_000314.6:c.1066_1067delinsTG	NP_000305.3:p.Asn356Cys
NM_001304717.2:c.1585_1586delinsTG	NP_001291646.2:p.Asn529Cys
NM_001304718.1:c.475_476delinsTG	NP_001291647.1:p.Asn159Cys
XM_006717926.2:c.1021_1022delinsTG	XP_006717989.1:p.Asn341Cys
XM_011539982.1:c.970_971delinsTG	XP_011538284.1:p.Asn324Cys
XR_945791.1:n.1636_1637delinsTG
NM_000314.7:c.1066_1067delinsTG	NP_000305.3:p.Asn356Cys
NM_001304717.5:c.1585_1586delinsTG	NP_001291646.4:p.Asn529Cys
NM_001304718.2:c.475_476delinsTG	NP_001291647.1:p.Asn159Cys
NM_000314.8:c.1066_1067delinsTG MANE Select	NP_000305.3:p.Asn356Cys