Canonical Allele Identifier: CA2610049789

Gene: PTEN

Linked Data

• gnomAD v4: 10-87966843-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966843G>T , CM000672.2:g.87966843G>T	GRCh38
NC_000010.10:g.89726600G>T , CM000672.1:g.89726600G>T	GRCh37
NC_000010.9:g.89716580G>T	NCBI36
NG_007466.2:g.108405G>T , LRG_311:g.108405G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.*1371G>T	ENSP00000514759.2:n.*1371G>T
ENST00000710265.1:c.*1612G>T	ENSP00000518161.1:n.*1612G>T
ENST00000688158.2:n.3318G>T
ENST00000688922.2:c.*2413G>T	ENSP00000508742.2:n.*2413G>T
ENST00000700021.1:c.*1371G>T	ENSP00000514757.1:n.*1371G>T
ENST00000700024.1:n.3975G>T
ENST00000706954.1:c.*1371G>T	ENSP00000516674.1:n.*1371G>T
ENST00000706955.1:c.*2618G>T	ENSP00000516675.1:n.*2618G>T
ENST00000688158.1:c.*2694G>T	ENSP00000509254.1:n.*2694G>T
ENST00000688308.1:c.*1371G>T	ENSP00000508752.1:n.*1371G>T
ENST00000688922.1:c.2504G>T
ENST00000693560.1:c.*1371G>T	ENSP00000509861.1:n.*1371G>T
ENST00000371953.8:c.*1371G>T MANE Select	ENSP00000361021.3:n.*1371G>T
ENST00000371953.7:c.*1371G>T	ENSP00000361021.3:n.*1371G>T
NM_000314.5:c.*1371G>T	NP_000305.3:n.*1371G>T
NM_000314.6:c.*1371G>T	NP_000305.3:n.*1371G>T
NM_001304717.2:c.*1371G>T	NP_001291646.2:n.*1371G>T
NM_001304718.1:c.*1371G>T	NP_001291647.1:n.*1371G>T
XM_006717926.2:c.*1371G>T	XP_006717989.1:n.*1371G>T
XM_011539982.1:c.*1371G>T	XP_011538284.1:n.*1371G>T
XR_945791.1:n.3153G>T
NM_000314.7:c.*1371G>T	NP_000305.3:n.*1371G>T
NM_001304717.5:c.*1371G>T	NP_001291646.4:n.*1371G>T
NM_001304718.2:c.*1371G>T	NP_001291647.1:n.*1371G>T
NM_000314.8:c.*1371G>T MANE Select	NP_000305.3:n.*1371G>T