Canonical Allele Identifier: CA2610049806

Gene: PTEN

Linked Data

• gnomAD v4: 10-87966927-T-TAA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966927_87966928insAA , CM000672.2:g.87966927_87966928insAA	GRCh38
NC_000010.10:g.89726684_89726685insAA , CM000672.1:g.89726684_89726685insAA	GRCh37
NC_000010.9:g.89716664_89716665insAA	NCBI36
NG_007466.2:g.108489_108490insAA , LRG_311:g.108489_108490insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1696_*1697insAA	ENSP00000518161.1:n.*1696_*1697insAA
ENST00000688158.2:n.3402_3403insAA
ENST00000706954.1:c.*1455_*1456insAA	ENSP00000516674.1:n.*1455_*1456insAA
ENST00000706955.1:c.*2702_*2703insAA	ENSP00000516675.1:n.*2702_*2703insAA
ENST00000688158.1:c.*2778_*2779insAA	ENSP00000509254.1:n.*2778_*2779insAA
ENST00000693560.1:c.*1455_*1456insAA	ENSP00000509861.1:n.*1455_*1456insAA
ENST00000371953.8:c.*1455_*1456insAA MANE Select	ENSP00000361021.3:n.*1455_*1456insAA
ENST00000371953.7:c.*1455_*1456insAA	ENSP00000361021.3:n.*1455_*1456insAA
NM_000314.5:c.*1455_*1456insAA	NP_000305.3:n.*1455_*1456insAA
NM_000314.6:c.*1455_*1456insAA	NP_000305.3:n.*1455_*1456insAA
NM_001304717.2:c.*1455_*1456insAA	NP_001291646.2:n.*1455_*1456insAA
NM_001304718.1:c.*1455_*1456insAA	NP_001291647.1:n.*1455_*1456insAA
XM_006717926.2:c.*1455_*1456insAA	XP_006717989.1:n.*1455_*1456insAA
XM_011539982.1:c.*1455_*1456insAA	XP_011538284.1:n.*1455_*1456insAA
XR_945791.1:n.3237_3238insAA
NM_000314.7:c.*1455_*1456insAA	NP_000305.3:n.*1455_*1456insAA
NM_001304717.5:c.*1455_*1456insAA	NP_001291646.4:n.*1455_*1456insAA
NM_001304718.2:c.*1455_*1456insAA	NP_001291647.1:n.*1455_*1456insAA
NM_000314.8:c.*1455_*1456insAA MANE Select	NP_000305.3:n.*1455_*1456insAA