Canonical Allele Identifier: CA2568302329

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967664_87967665insG , CM000672.2:g.87967664_87967665insG	GRCh38
NC_000010.10:g.89727421_89727422insG , CM000672.1:g.89727421_89727422insG	GRCh37
NC_000010.9:g.89717401_89717402insG	NCBI36
NG_007466.2:g.109226_109227insG , LRG_311:g.109226_109227insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*2433_*2434insG	ENSP00000518161.1:n.*2433_*2434insG
ENST00000688158.2:n.4139_4140insG
ENST00000706954.1:c.*2192_*2193insG	ENSP00000516674.1:n.*2192_*2193insG
ENST00000706955.1:c.*3439_*3440insG	ENSP00000516675.1:n.*3439_*3440insG
ENST00000688158.1:c.*3515_*3516insG	ENSP00000509254.1:n.*3515_*3516insG
ENST00000693560.1:c.*2192_*2193insG	ENSP00000509861.1:n.*2192_*2193insG
ENST00000371953.8:c.*2192_*2193insG MANE Select	ENSP00000361021.3:n.*2192_*2193insG
ENST00000371953.7:c.*2192_*2193insG	ENSP00000361021.3:n.*2192_*2193insG
NM_000314.5:c.*2192_*2193insG	NP_000305.3:n.*2192_*2193insG
NM_000314.6:c.*2192_*2193insG	NP_000305.3:n.*2192_*2193insG
NM_001304717.2:c.*2192_*2193insG	NP_001291646.2:n.*2192_*2193insG
NM_001304718.1:c.*2192_*2193insG	NP_001291647.1:n.*2192_*2193insG
XM_006717926.2:c.*2192_*2193insG	XP_006717989.1:n.*2192_*2193insG
XM_011539982.1:c.*2192_*2193insG	XP_011538284.1:n.*2192_*2193insG
XR_945791.1:n.3974_3975insG
NM_000314.7:c.*2192_*2193insG	NP_000305.3:n.*2192_*2193insG
NM_001304717.5:c.*2192_*2193insG	NP_001291646.4:n.*2192_*2193insG
NM_001304718.2:c.*2192_*2193insG	NP_001291647.1:n.*2192_*2193insG
NM_000314.8:c.*2192_*2193insG MANE Select	NP_000305.3:n.*2192_*2193insG