Canonical Allele Identifier: CA891837205

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965326_87965327delinsGG , CM000672.2:g.87965326_87965327delinsGG	GRCh38
NC_000010.10:g.89725083_89725084delinsGG , CM000672.1:g.89725083_89725084delinsGG	GRCh37
NC_000010.9:g.89715063_89715064delinsGG	NCBI36
NG_007466.2:g.106888_106889delinsGG , LRG_311:g.106888_106889delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1159_1160delinsGG	ENSP00000514759.2:p.Asn387Gly
ENST00000710265.1:c.*95_*96delinsGG	ENSP00000518161.1:n.*95_*96delinsGG
ENST00000688158.2:n.1801_1802delinsGG
ENST00000688922.2:c.*896_*897delinsGG	ENSP00000508742.2:n.*896_*897delinsGG
ENST00000700021.1:c.1021_1022delinsGG	ENSP00000514757.1:p.Asn341Gly
ENST00000700022.1:c.*405_*406delinsGG	ENSP00000514758.1:n.*405_*406delinsGG
ENST00000700023.1:n.2224_2225delinsGG
ENST00000700024.1:n.2458_2459delinsGG
ENST00000706954.1:c.1066_1067delinsGG	ENSP00000516674.1:p.Asn356Gly
ENST00000706955.1:c.*1101_*1102delinsGG	ENSP00000516675.1:n.*1101_*1102delinsGG
ENST00000686459.1:c.*652_*653delinsGG	ENSP00000508909.1:n.*652_*653delinsGG
ENST00000688158.1:c.*1177_*1178delinsGG	ENSP00000509254.1:n.*1177_*1178delinsGG
ENST00000688308.1:c.1066_1067delinsGG	ENSP00000508752.1:p.Asn356Gly
ENST00000688922.1:c.987_988delinsGG
ENST00000693560.1:c.1585_1586delinsGG	ENSP00000509861.1:p.Asn529Gly
ENST00000371953.8:c.1066_1067delinsGG MANE Select	ENSP00000361021.3:p.Asn356Gly
ENST00000371953.7:c.1066_1067delinsGG	ENSP00000361021.3:p.Asn356Gly
NM_000314.5:c.1066_1067delinsGG	NP_000305.3:p.Asn356Gly
NM_000314.6:c.1066_1067delinsGG	NP_000305.3:p.Asn356Gly
NM_001304717.2:c.1585_1586delinsGG	NP_001291646.2:p.Asn529Gly
NM_001304718.1:c.475_476delinsGG	NP_001291647.1:p.Asn159Gly
XM_006717926.2:c.1021_1022delinsGG	XP_006717989.1:p.Asn341Gly
XM_011539982.1:c.970_971delinsGG	XP_011538284.1:p.Asn324Gly
XR_945791.1:n.1636_1637delinsGG
NM_000314.7:c.1066_1067delinsGG	NP_000305.3:p.Asn356Gly
NM_001304717.5:c.1585_1586delinsGG	NP_001291646.4:p.Asn529Gly
NM_001304718.2:c.475_476delinsGG	NP_001291647.1:p.Asn159Gly
NM_000314.8:c.1066_1067delinsGG MANE Select	NP_000305.3:p.Asn356Gly