Canonical Allele Identifier: CA2610049800

Gene: PTEN

Linked Data

• gnomAD v4: 10-87966906-T-TCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966906_87966907insCTG , CM000672.2:g.87966906_87966907insCTG	GRCh38
NC_000010.10:g.89726663_89726664insCTG , CM000672.1:g.89726663_89726664insCTG	GRCh37
NC_000010.9:g.89716643_89716644insCTG	NCBI36
NG_007466.2:g.108468_108469insCTG , LRG_311:g.108468_108469insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1675_*1676insCTG	ENSP00000518161.1:n.*1675_*1676insCTG
ENST00000688158.2:n.3381_3382insCTG
ENST00000706954.1:c.*1434_*1435insCTG	ENSP00000516674.1:n.*1434_*1435insCTG
ENST00000706955.1:c.*2681_*2682insCTG	ENSP00000516675.1:n.*2681_*2682insCTG
ENST00000688158.1:c.*2757_*2758insCTG	ENSP00000509254.1:n.*2757_*2758insCTG
ENST00000693560.1:c.*1434_*1435insCTG	ENSP00000509861.1:n.*1434_*1435insCTG
ENST00000371953.8:c.*1434_*1435insCTG MANE Select	ENSP00000361021.3:n.*1434_*1435insCTG
ENST00000371953.7:c.*1434_*1435insCTG	ENSP00000361021.3:n.*1434_*1435insCTG
NM_000314.5:c.*1434_*1435insCTG	NP_000305.3:n.*1434_*1435insCTG
NM_000314.6:c.*1434_*1435insCTG	NP_000305.3:n.*1434_*1435insCTG
NM_001304717.2:c.*1434_*1435insCTG	NP_001291646.2:n.*1434_*1435insCTG
NM_001304718.1:c.*1434_*1435insCTG	NP_001291647.1:n.*1434_*1435insCTG
XM_006717926.2:c.*1434_*1435insCTG	XP_006717989.1:n.*1434_*1435insCTG
XM_011539982.1:c.*1434_*1435insCTG	XP_011538284.1:n.*1434_*1435insCTG
XR_945791.1:n.3216_3217insCTG
NM_000314.7:c.*1434_*1435insCTG	NP_000305.3:n.*1434_*1435insCTG
NM_001304717.5:c.*1434_*1435insCTG	NP_001291646.4:n.*1434_*1435insCTG
NM_001304718.2:c.*1434_*1435insCTG	NP_001291647.1:n.*1434_*1435insCTG
NM_000314.8:c.*1434_*1435insCTG MANE Select	NP_000305.3:n.*1434_*1435insCTG