Canonical Allele Identifier: CA211259996

Gene: PTEN

Linked Data

• dbSNP Id: rs952642365
• gnomAD v2: 10-89726647-TGAAA-T
• gnomAD v3: 10-87966890-TGAAA-T
• gnomAD v4: 10-87966890-TGAAA-T
• MyVariant Identifiers: chr10:g.89726648_89726651del (hg19) ; chr10:g.87966891_87966894del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966894_87966897del , CM000672.2:g.87966894_87966897del	GRCh38
NC_000010.10:g.89726651_89726654del , CM000672.1:g.89726651_89726654del	GRCh37
NC_000010.9:g.89716631_89716634del	NCBI36
NG_007466.2:g.108456_108459del , LRG_311:g.108456_108459del

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*1663_*1666del	ENSP00000518161.1:n.*1663_*1666del
ENST00000688158.2:n.3369_3372del
ENST00000706954.1:c.*1422_*1425del	ENSP00000516674.1:n.*1422_*1425del
ENST00000706955.1:c.*2669_*2672del	ENSP00000516675.1:n.*2669_*2672del
ENST00000688158.1:c.*2745_*2748del	ENSP00000509254.1:n.*2745_*2748del
ENST00000693560.1:c.*1422_*1425del	ENSP00000509861.1:n.*1422_*1425del
ENST00000371953.8:c.*1422_*1425del MANE Select	ENSP00000361021.3:n.*1422_*1425del
ENST00000371953.7:c.*1422_*1425del	ENSP00000361021.3:n.*1422_*1425del
NM_000314.5:c.*1422_*1425del	NP_000305.3:n.*1422_*1425del
NM_000314.6:c.*1422_*1425del	NP_000305.3:n.*1422_*1425del
NM_001304717.2:c.*1422_*1425del	NP_001291646.2:n.*1422_*1425del
NM_001304718.1:c.*1422_*1425del	NP_001291647.1:n.*1422_*1425del
XM_006717926.2:c.*1422_*1425del	XP_006717989.1:n.*1422_*1425del
XM_011539982.1:c.*1422_*1425del	XP_011538284.1:n.*1422_*1425del
XR_945791.1:n.3204_3207del
NM_000314.7:c.*1422_*1425del	NP_000305.3:n.*1422_*1425del
NM_001304717.5:c.*1422_*1425del	NP_001291646.4:n.*1422_*1425del
NM_001304718.2:c.*1422_*1425del	NP_001291647.1:n.*1422_*1425del
NM_000314.8:c.*1422_*1425del MANE Select	NP_000305.3:n.*1422_*1425del