Canonical Allele Identifier: CA891839342

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957862_87957863delinsGG , CM000672.2:g.87957862_87957863delinsGG	GRCh38
NC_000010.10:g.89717619_89717620delinsGG , CM000672.1:g.89717619_89717620delinsGG	GRCh37
NC_000010.9:g.89707599_89707600delinsGG	NCBI36
NG_007466.2:g.99424_99425delinsGG , LRG_311:g.99424_99425delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.644_645delinsGG	ENSP00000514759.2:p.Phe215Trp
ENST00000710265.1:c.644_645delinsGG	ENSP00000518161.1:p.Phe215Trp
ENST00000472832.3:c.644_645delinsGG	ENSP00000483066.2:p.Phe215Trp
ENST00000688158.2:n.1379_1380delinsGG
ENST00000688922.2:c.*474_*475delinsGG	ENSP00000508742.2:n.*474_*475delinsGG
ENST00000700021.1:c.599_600delinsGG	ENSP00000514757.1:p.Phe200Trp
ENST00000700022.1:c.502_503delinsGG	ENSP00000514758.1:p.Leu168Gly
ENST00000700023.1:n.1802_1803delinsGG
ENST00000700024.1:n.2036_2037delinsGG
ENST00000700025.1:n.1413_1414delinsGG
ENST00000700026.1:n.281_282delinsGG
ENST00000700029.1:c.478_479delinsGG
ENST00000706954.1:c.644_645delinsGG	ENSP00000516674.1:p.Phe215Trp
ENST00000706955.1:c.*679_*680delinsGG	ENSP00000516675.1:n.*679_*680delinsGG
ENST00000686459.1:c.*230_*231delinsGG	ENSP00000508909.1:n.*230_*231delinsGG
ENST00000688158.1:c.*755_*756delinsGG	ENSP00000509254.1:n.*755_*756delinsGG
ENST00000688308.1:c.644_645delinsGG	ENSP00000508752.1:p.Phe215Trp
ENST00000688922.1:c.565_566delinsGG
ENST00000693560.1:c.1163_1164delinsGG	ENSP00000509861.1:p.Phe388Trp
ENST00000371953.8:c.644_645delinsGG MANE Select	ENSP00000361021.3:p.Phe215Trp
ENST00000371953.7:c.644_645delinsGG	ENSP00000361021.3:p.Phe215Trp
ENST00000472832.2:c.71_72delinsGG	ENSP00000483066.1:p.Phe24Trp
NM_000314.5:c.644_645delinsGG	NP_000305.3:p.Phe215Trp
NM_000314.6:c.644_645delinsGG	NP_000305.3:p.Phe215Trp
NM_001304717.2:c.1163_1164delinsGG	NP_001291646.2:p.Phe388Trp
NM_001304718.1:c.53_54delinsGG	NP_001291647.1:p.Phe18Trp
XM_006717926.2:c.599_600delinsGG	XP_006717989.1:p.Phe200Trp
XM_011539981.1:c.644_645delinsGG	XP_011538283.1:p.Phe215Trp
XM_011539982.1:c.548_549delinsGG	XP_011538284.1:p.Phe183Trp
XR_945791.1:n.1214_1215delinsGG
NM_000314.7:c.644_645delinsGG	NP_000305.3:p.Phe215Trp
NM_001304717.5:c.1163_1164delinsGG	NP_001291646.4:p.Phe388Trp
NM_001304718.2:c.53_54delinsGG	NP_001291647.1:p.Phe18Trp
NM_000314.8:c.644_645delinsGG MANE Select	NP_000305.3:p.Phe215Trp