Canonical Allele Identifier: CA930910771

Gene: PTEN

Linked Data

• dbSNP Id: rs1860779626
• gnomAD v3: 10-87966912-T-TTTC
• gnomAD v4: 10-87966912-T-TTTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966914_87966915insCTT , CM000672.2:g.87966914_87966915insCTT	GRCh38
NC_000010.10:g.89726671_89726672insCTT , CM000672.1:g.89726671_89726672insCTT	GRCh37
NC_000010.9:g.89716651_89716652insCTT	NCBI36
NG_007466.2:g.108476_108477insCTT , LRG_311:g.108476_108477insCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1683_*1684insCTT	ENSP00000518161.1:n.*1683_*1684insCTT
ENST00000688158.2:n.3389_3390insCTT
ENST00000706954.1:c.*1442_*1443insCTT	ENSP00000516674.1:n.*1442_*1443insCTT
ENST00000706955.1:c.*2689_*2690insCTT	ENSP00000516675.1:n.*2689_*2690insCTT
ENST00000688158.1:c.*2765_*2766insCTT	ENSP00000509254.1:n.*2765_*2766insCTT
ENST00000693560.1:c.*1442_*1443insCTT	ENSP00000509861.1:n.*1442_*1443insCTT
ENST00000371953.8:c.*1442_*1443insCTT MANE Select	ENSP00000361021.3:n.*1442_*1443insCTT
ENST00000371953.7:c.*1442_*1443insCTT	ENSP00000361021.3:n.*1442_*1443insCTT
NM_000314.5:c.*1442_*1443insCTT	NP_000305.3:n.*1442_*1443insCTT
NM_000314.6:c.*1442_*1443insCTT	NP_000305.3:n.*1442_*1443insCTT
NM_001304717.2:c.*1442_*1443insCTT	NP_001291646.2:n.*1442_*1443insCTT
NM_001304718.1:c.*1442_*1443insCTT	NP_001291647.1:n.*1442_*1443insCTT
XM_006717926.2:c.*1442_*1443insCTT	XP_006717989.1:n.*1442_*1443insCTT
XM_011539982.1:c.*1442_*1443insCTT	XP_011538284.1:n.*1442_*1443insCTT
XR_945791.1:n.3224_3225insCTT
NM_000314.7:c.*1442_*1443insCTT	NP_000305.3:n.*1442_*1443insCTT
NM_001304717.5:c.*1442_*1443insCTT	NP_001291646.4:n.*1442_*1443insCTT
NM_001304718.2:c.*1442_*1443insCTT	NP_001291647.1:n.*1442_*1443insCTT
NM_000314.8:c.*1442_*1443insCTT MANE Select	NP_000305.3:n.*1442_*1443insCTT