Canonical Allele Identifier: CA669574393

Gene: PTEN

Linked Data

• dbSNP Id: rs1554826208
• MyVariant Identifiers: chr10:g.87966913_87966914insTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966914_87966915insGT , CM000672.2:g.87966914_87966915insGT	GRCh38
NC_000010.10:g.89726671_89726672insGT , CM000672.1:g.89726671_89726672insGT	GRCh37
NC_000010.9:g.89716651_89716652insGT	NCBI36
NG_007466.2:g.108476_108477insGT , LRG_311:g.108476_108477insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1683_*1684insGT	ENSP00000518161.1:n.*1683_*1684insGT
ENST00000688158.2:n.3389_3390insGT
ENST00000706954.1:c.*1442_*1443insGT	ENSP00000516674.1:n.*1442_*1443insGT
ENST00000706955.1:c.*2689_*2690insGT	ENSP00000516675.1:n.*2689_*2690insGT
ENST00000688158.1:c.*2765_*2766insGT	ENSP00000509254.1:n.*2765_*2766insGT
ENST00000693560.1:c.*1442_*1443insGT	ENSP00000509861.1:n.*1442_*1443insGT
ENST00000371953.8:c.*1442_*1443insGT MANE Select	ENSP00000361021.3:n.*1442_*1443insGT
ENST00000371953.7:c.*1442_*1443insGT	ENSP00000361021.3:n.*1442_*1443insGT
NM_000314.5:c.*1442_*1443insGT	NP_000305.3:n.*1442_*1443insGT
NM_000314.6:c.*1442_*1443insGT	NP_000305.3:n.*1442_*1443insGT
NM_001304717.2:c.*1442_*1443insGT	NP_001291646.2:n.*1442_*1443insGT
NM_001304718.1:c.*1442_*1443insGT	NP_001291647.1:n.*1442_*1443insGT
XM_006717926.2:c.*1442_*1443insGT	XP_006717989.1:n.*1442_*1443insGT
XM_011539982.1:c.*1442_*1443insGT	XP_011538284.1:n.*1442_*1443insGT
XR_945791.1:n.3224_3225insGT
NM_000314.7:c.*1442_*1443insGT	NP_000305.3:n.*1442_*1443insGT
NM_001304717.5:c.*1442_*1443insGT	NP_001291646.4:n.*1442_*1443insGT
NM_001304718.2:c.*1442_*1443insGT	NP_001291647.1:n.*1442_*1443insGT
NM_000314.8:c.*1442_*1443insGT MANE Select	NP_000305.3:n.*1442_*1443insGT