Canonical Allele Identifier: CA1926177529

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967927_87967928delinsAT , CM000672.2:g.87967927_87967928delinsAT	GRCh38
NC_000010.10:g.89727684_89727685delinsAT , CM000672.1:g.89727684_89727685delinsAT	GRCh37
NC_000010.9:g.89717664_89717665delinsAT	NCBI36
NG_007466.2:g.109489_109490delinsAT , LRG_311:g.109489_109490delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*2696_*2697delinsAT	ENSP00000518161.1:n.*2696_*2697delinsAT
ENST00000688158.2:n.4402_4403delinsAT
ENST00000706954.1:c.*2455_*2456delinsAT	ENSP00000516674.1:n.*2455_*2456delinsAT
ENST00000706955.1:c.*3702_*3703delinsAT	ENSP00000516675.1:n.*3702_*3703delinsAT
ENST00000688158.1:c.*3778_*3779delinsAT	ENSP00000509254.1:n.*3778_*3779delinsAT
ENST00000693560.1:c.*2455_*2456delinsAT	ENSP00000509861.1:n.*2455_*2456delinsAT
ENST00000371953.8:c.*2455_*2456delinsAT MANE Select	ENSP00000361021.3:n.*2455_*2456delinsAT
ENST00000371953.7:c.*2455_*2456delinsAT	ENSP00000361021.3:n.*2455_*2456delinsAT
NM_000314.5:c.*2455_*2456delinsAT	NP_000305.3:n.*2455_*2456delinsAT
NM_000314.6:c.*2455_*2456delinsAT	NP_000305.3:n.*2455_*2456delinsAT
NM_001304717.2:c.*2455_*2456delinsAT	NP_001291646.2:n.*2455_*2456delinsAT
NM_001304718.1:c.*2455_*2456delinsAT	NP_001291647.1:n.*2455_*2456delinsAT
XM_006717926.2:c.*2455_*2456delinsAT	XP_006717989.1:n.*2455_*2456delinsAT
XM_011539982.1:c.*2455_*2456delinsAT	XP_011538284.1:n.*2455_*2456delinsAT
XR_945791.1:n.4237_4238delinsAT
NM_000314.7:c.*2455_*2456delinsAT	NP_000305.3:n.*2455_*2456delinsAT
NM_001304717.5:c.*2455_*2456delinsAT	NP_001291646.4:n.*2455_*2456delinsAT
NM_001304718.2:c.*2455_*2456delinsAT	NP_001291647.1:n.*2455_*2456delinsAT
NM_000314.8:c.*2455_*2456delinsAT MANE Select	NP_000305.3:n.*2455_*2456delinsAT