Canonical Allele Identifier: CA211259854

Gene: PTEN

Linked Data

• dbSNP Id: rs902882242
• gnomAD v2: 10-89726541-TAAA-T
• gnomAD v3: 10-87966784-TAAA-T
• gnomAD v4: 10-87966784-TAAA-T
• MyVariant Identifiers: chr10:g.89726542_89726544del (hg19) ; chr10:g.87966785_87966787del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966787_87966789del , CM000672.2:g.87966787_87966789del	GRCh38
NC_000010.10:g.89726544_89726546del , CM000672.1:g.89726544_89726546del	GRCh37
NC_000010.9:g.89716524_89716526del	NCBI36
NG_007466.2:g.108349_108351del , LRG_311:g.108349_108351del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.*1315_*1317del	ENSP00000514759.2:n.*1315_*1317del
ENST00000710265.1:c.*1556_*1558del	ENSP00000518161.1:n.*1556_*1558del
ENST00000688158.2:n.3262_3264del
ENST00000688922.2:c.*2357_*2359del	ENSP00000508742.2:n.*2357_*2359del
ENST00000700021.1:c.*1315_*1317del	ENSP00000514757.1:n.*1315_*1317del
ENST00000700022.1:c.*1866_*1868del	ENSP00000514758.1:n.*1866_*1868del
ENST00000700024.1:n.3919_3921del
ENST00000706954.1:c.*1315_*1317del	ENSP00000516674.1:n.*1315_*1317del
ENST00000706955.1:c.*2562_*2564del	ENSP00000516675.1:n.*2562_*2564del
ENST00000688158.1:c.*2638_*2640del	ENSP00000509254.1:n.*2638_*2640del
ENST00000688308.1:c.*1315_*1317del	ENSP00000508752.1:n.*1315_*1317del
ENST00000688922.1:c.2448_2450del
ENST00000693560.1:c.*1315_*1317del	ENSP00000509861.1:n.*1315_*1317del
ENST00000371953.8:c.*1315_*1317del MANE Select	ENSP00000361021.3:n.*1315_*1317del
ENST00000371953.7:c.*1315_*1317del	ENSP00000361021.3:n.*1315_*1317del
NM_000314.5:c.*1315_*1317del	NP_000305.3:n.*1315_*1317del
NM_000314.6:c.*1315_*1317del	NP_000305.3:n.*1315_*1317del
NM_001304717.2:c.*1315_*1317del	NP_001291646.2:n.*1315_*1317del
NM_001304718.1:c.*1315_*1317del	NP_001291647.1:n.*1315_*1317del
XM_006717926.2:c.*1315_*1317del	XP_006717989.1:n.*1315_*1317del
XM_011539982.1:c.*1315_*1317del	XP_011538284.1:n.*1315_*1317del
XR_945791.1:n.3097_3099del
NM_000314.7:c.*1315_*1317del	NP_000305.3:n.*1315_*1317del
NM_001304717.5:c.*1315_*1317del	NP_001291646.4:n.*1315_*1317del
NM_001304718.2:c.*1315_*1317del	NP_001291647.1:n.*1315_*1317del
NM_000314.8:c.*1315_*1317del MANE Select	NP_000305.3:n.*1315_*1317del