Canonical Allele Identifier: CA2523217682

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966903_87966904insC , CM000672.2:g.87966903_87966904insC	GRCh38
NC_000010.10:g.89726660_89726661insC , CM000672.1:g.89726660_89726661insC	GRCh37
NC_000010.9:g.89716640_89716641insC	NCBI36
NG_007466.2:g.108465_108466insC , LRG_311:g.108465_108466insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1672_*1673insC	ENSP00000518161.1:n.*1672_*1673insC
ENST00000688158.2:n.3378_3379insC
ENST00000706954.1:c.*1431_*1432insC	ENSP00000516674.1:n.*1431_*1432insC
ENST00000706955.1:c.*2678_*2679insC	ENSP00000516675.1:n.*2678_*2679insC
ENST00000688158.1:c.*2754_*2755insC	ENSP00000509254.1:n.*2754_*2755insC
ENST00000693560.1:c.*1431_*1432insC	ENSP00000509861.1:n.*1431_*1432insC
ENST00000371953.8:c.*1431_*1432insC MANE Select	ENSP00000361021.3:n.*1431_*1432insC
ENST00000371953.7:c.*1431_*1432insC	ENSP00000361021.3:n.*1431_*1432insC
NM_000314.5:c.*1431_*1432insC	NP_000305.3:n.*1431_*1432insC
NM_000314.6:c.*1431_*1432insC	NP_000305.3:n.*1431_*1432insC
NM_001304717.2:c.*1431_*1432insC	NP_001291646.2:n.*1431_*1432insC
NM_001304718.1:c.*1431_*1432insC	NP_001291647.1:n.*1431_*1432insC
XM_006717926.2:c.*1431_*1432insC	XP_006717989.1:n.*1431_*1432insC
XM_011539982.1:c.*1431_*1432insC	XP_011538284.1:n.*1431_*1432insC
XR_945791.1:n.3213_3214insC
NM_000314.7:c.*1431_*1432insC	NP_000305.3:n.*1431_*1432insC
NM_001304717.5:c.*1431_*1432insC	NP_001291646.4:n.*1431_*1432insC
NM_001304718.2:c.*1431_*1432insC	NP_001291647.1:n.*1431_*1432insC
NM_000314.8:c.*1431_*1432insC MANE Select	NP_000305.3:n.*1431_*1432insC