Canonical Allele Identifier: CA1926177667

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87968020_87968032delinsTAGGTAATCTCTG , CM000672.2:g.87968020_87968032delinsTAGGTAATCTCTG	GRCh38
NC_000010.10:g.89727777_89727789delinsTAGGTAATCTCTG , CM000672.1:g.89727777_89727789delinsTAGGTAATCTCTG	GRCh37
NC_000010.9:g.89717757_89717769delinsTAGGTAATCTCTG	NCBI36
NG_007466.2:g.109582_109594delinsTAGGTAATCTCTG , LRG_311:g.109582_109594delinsTAGGTAATCTCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*2789_*2801delinsTAGGTAATCTCTG	ENSP00000518161.1:n.*2789_*2801delinsTAGGTAATCTCTG
ENST00000688158.2:n.4495_4507delinsTAGGTAATCTCTG
ENST00000706954.1:c.*2548_*2560delinsTAGGTAATCTCTG	ENSP00000516674.1:n.*2548_*2560delinsTAGGTAATCTCTG
ENST00000706955.1:c.*3795_*3807delinsTAGGTAATCTCTG	ENSP00000516675.1:n.*3795_*3807delinsTAGGTAATCTCTG
ENST00000688158.1:c.*3871_*3883delinsTAGGTAATCTCTG	ENSP00000509254.1:n.*3871_*3883delinsTAGGTAATCTCTG
ENST00000693560.1:c.*2548_*2560delinsTAGGTAATCTCTG	ENSP00000509861.1:n.*2548_*2560delinsTAGGTAATCTCTG
ENST00000371953.8:c.*2548_*2560delinsTAGGTAATCTCTG MANE Select	ENSP00000361021.3:n.*2548_*2560delinsTAGGTAATCTCTG
ENST00000371953.7:c.*2548_*2560delinsTAGGTAATCTCTG	ENSP00000361021.3:n.*2548_*2560delinsTAGGTAATCTCTG
NM_000314.5:c.*2548_*2560delinsTAGGTAATCTCTG	NP_000305.3:n.*2548_*2560delinsTAGGTAATCTCTG
NM_000314.6:c.*2548_*2560delinsTAGGTAATCTCTG	NP_000305.3:n.*2548_*2560delinsTAGGTAATCTCTG
NM_001304717.2:c.*2548_*2560delinsTAGGTAATCTCTG	NP_001291646.2:n.*2548_*2560delinsTAGGTAATCTCTG
NM_001304718.1:c.*2548_*2560delinsTAGGTAATCTCTG	NP_001291647.1:n.*2548_*2560delinsTAGGTAATCTCTG
XM_006717926.2:c.*2548_*2560delinsTAGGTAATCTCTG	XP_006717989.1:n.*2548_*2560delinsTAGGTAATCTCTG
XM_011539982.1:c.*2548_*2560delinsTAGGTAATCTCTG	XP_011538284.1:n.*2548_*2560delinsTAGGTAATCTCTG
XR_945791.1:n.4330_4342delinsTAGGTAATCTCTG
NM_000314.7:c.*2548_*2560delinsTAGGTAATCTCTG	NP_000305.3:n.*2548_*2560delinsTAGGTAATCTCTG
NM_001304717.5:c.*2548_*2560delinsTAGGTAATCTCTG	NP_001291646.4:n.*2548_*2560delinsTAGGTAATCTCTG
NM_001304718.2:c.*2548_*2560delinsTAGGTAATCTCTG	NP_001291647.1:n.*2548_*2560delinsTAGGTAATCTCTG
NM_000314.8:c.*2548_*2560delinsTAGGTAATCTCTG MANE Select	NP_000305.3:n.*2548_*2560delinsTAGGTAATCTCTG