Canonical Allele Identifier: CA2610049813

Gene: PTEN

Linked Data

• gnomAD v4: 10-87966937-TGCAGTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966938_87966943del , CM000672.2:g.87966938_87966943del	GRCh38
NC_000010.10:g.89726695_89726700del , CM000672.1:g.89726695_89726700del	GRCh37
NC_000010.9:g.89716675_89716680del	NCBI36
NG_007466.2:g.108500_108505del , LRG_311:g.108500_108505del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1707_*1712del	ENSP00000518161.1:n.*1707_*1712del
ENST00000688158.2:n.3413_3418del
ENST00000706954.1:c.*1466_*1471del	ENSP00000516674.1:n.*1466_*1471del
ENST00000706955.1:c.*2713_*2718del	ENSP00000516675.1:n.*2713_*2718del
ENST00000688158.1:c.*2789_*2794del	ENSP00000509254.1:n.*2789_*2794del
ENST00000693560.1:c.*1466_*1471del	ENSP00000509861.1:n.*1466_*1471del
ENST00000371953.8:c.*1466_*1471del MANE Select	ENSP00000361021.3:n.*1466_*1471del
ENST00000371953.7:c.*1466_*1471del	ENSP00000361021.3:n.*1466_*1471del
NM_000314.5:c.*1466_*1471del	NP_000305.3:n.*1466_*1471del
NM_000314.6:c.*1466_*1471del	NP_000305.3:n.*1466_*1471del
NM_001304717.2:c.*1466_*1471del	NP_001291646.2:n.*1466_*1471del
NM_001304718.1:c.*1466_*1471del	NP_001291647.1:n.*1466_*1471del
XM_006717926.2:c.*1466_*1471del	XP_006717989.1:n.*1466_*1471del
XM_011539982.1:c.*1466_*1471del	XP_011538284.1:n.*1466_*1471del
XR_945791.1:n.3248_3253del
NM_000314.7:c.*1466_*1471del	NP_000305.3:n.*1466_*1471del
NM_001304717.5:c.*1466_*1471del	NP_001291646.4:n.*1466_*1471del
NM_001304718.2:c.*1466_*1471del	NP_001291647.1:n.*1466_*1471del
NM_000314.8:c.*1466_*1471del MANE Select	NP_000305.3:n.*1466_*1471del