Canonical Allele Identifier: CA1926177702

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87968030_87968032delinsCTG , CM000672.2:g.87968030_87968032delinsCTG	GRCh38
NC_000010.10:g.89727787_89727789delinsCTG , CM000672.1:g.89727787_89727789delinsCTG	GRCh37
NC_000010.9:g.89717767_89717769delinsCTG	NCBI36
NG_007466.2:g.109592_109594delinsCTG , LRG_311:g.109592_109594delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*2799_*2801delinsCTG	ENSP00000518161.1:n.*2799_*2801delinsCTG
ENST00000688158.2:n.4505_4507delinsCTG
ENST00000706954.1:c.*2558_*2560delinsCTG	ENSP00000516674.1:n.*2558_*2560delinsCTG
ENST00000706955.1:c.*3805_*3807delinsCTG	ENSP00000516675.1:n.*3805_*3807delinsCTG
ENST00000688158.1:c.*3881_*3883delinsCTG	ENSP00000509254.1:n.*3881_*3883delinsCTG
ENST00000693560.1:c.*2558_*2560delinsCTG	ENSP00000509861.1:n.*2558_*2560delinsCTG
ENST00000371953.8:c.*2558_*2560delinsCTG MANE Select	ENSP00000361021.3:n.*2558_*2560delinsCTG
ENST00000371953.7:c.*2558_*2560delinsCTG	ENSP00000361021.3:n.*2558_*2560delinsCTG
NM_000314.5:c.*2558_*2560delinsCTG	NP_000305.3:n.*2558_*2560delinsCTG
NM_000314.6:c.*2558_*2560delinsCTG	NP_000305.3:n.*2558_*2560delinsCTG
NM_001304717.2:c.*2558_*2560delinsCTG	NP_001291646.2:n.*2558_*2560delinsCTG
NM_001304718.1:c.*2558_*2560delinsCTG	NP_001291647.1:n.*2558_*2560delinsCTG
XM_006717926.2:c.*2558_*2560delinsCTG	XP_006717989.1:n.*2558_*2560delinsCTG
XM_011539982.1:c.*2558_*2560delinsCTG	XP_011538284.1:n.*2558_*2560delinsCTG
XR_945791.1:n.4340_4342delinsCTG
NM_000314.7:c.*2558_*2560delinsCTG	NP_000305.3:n.*2558_*2560delinsCTG
NM_001304717.5:c.*2558_*2560delinsCTG	NP_001291646.4:n.*2558_*2560delinsCTG
NM_001304718.2:c.*2558_*2560delinsCTG	NP_001291647.1:n.*2558_*2560delinsCTG
NM_000314.8:c.*2558_*2560delinsCTG MANE Select	NP_000305.3:n.*2558_*2560delinsCTG