Canonical Allele Identifier: CA1926175877

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966921_87966932delinsTTTTTTTTTTTA , CM000672.2:g.87966921_87966932delinsTTTTTTTTTTTA	GRCh38
NC_000010.10:g.89726678_89726689delinsTTTTTTTTTTTA , CM000672.1:g.89726678_89726689delinsTTTTTTTTTTTA	GRCh37
NC_000010.9:g.89716658_89716669delinsTTTTTTTTTTTA	NCBI36
NG_007466.2:g.108483_108494delinsTTTTTTTTTTTA , LRG_311:g.108483_108494delinsTTTTTTTTTTTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*1690_*1701delinsTTTTTTTTTTTA	ENSP00000518161.1:n.*1690_*1701delinsTTTTTTTTTTTA
ENST00000688158.2:n.3396_3407delinsTTTTTTTTTTTA
ENST00000706954.1:c.*1449_*1460delinsTTTTTTTTTTTA	ENSP00000516674.1:n.*1449_*1460delinsTTTTTTTTTTTA
ENST00000706955.1:c.*2696_*2707delinsTTTTTTTTTTTA	ENSP00000516675.1:n.*2696_*2707delinsTTTTTTTTTTTA
ENST00000688158.1:c.*2772_*2783delinsTTTTTTTTTTTA	ENSP00000509254.1:n.*2772_*2783delinsTTTTTTTTTTTA
ENST00000693560.1:c.*1449_*1460delinsTTTTTTTTTTTA	ENSP00000509861.1:n.*1449_*1460delinsTTTTTTTTTTTA
ENST00000371953.8:c.*1449_*1460delinsTTTTTTTTTTTA MANE Select	ENSP00000361021.3:n.*1449_*1460delinsTTTTTTTTTTTA
ENST00000371953.7:c.*1449_*1460delinsTTTTTTTTTTTA	ENSP00000361021.3:n.*1449_*1460delinsTTTTTTTTTTTA
NM_000314.5:c.*1449_*1460delinsTTTTTTTTTTTA	NP_000305.3:n.*1449_*1460delinsTTTTTTTTTTTA
NM_000314.6:c.*1449_*1460delinsTTTTTTTTTTTA	NP_000305.3:n.*1449_*1460delinsTTTTTTTTTTTA
NM_001304717.2:c.*1449_*1460delinsTTTTTTTTTTTA	NP_001291646.2:n.*1449_*1460delinsTTTTTTTTTTTA
NM_001304718.1:c.*1449_*1460delinsTTTTTTTTTTTA	NP_001291647.1:n.*1449_*1460delinsTTTTTTTTTTTA
XM_006717926.2:c.*1449_*1460delinsTTTTTTTTTTTA	XP_006717989.1:n.*1449_*1460delinsTTTTTTTTTTTA
XM_011539982.1:c.*1449_*1460delinsTTTTTTTTTTTA	XP_011538284.1:n.*1449_*1460delinsTTTTTTTTTTTA
XR_945791.1:n.3231_3242delinsTTTTTTTTTTTA
NM_000314.7:c.*1449_*1460delinsTTTTTTTTTTTA	NP_000305.3:n.*1449_*1460delinsTTTTTTTTTTTA
NM_001304717.5:c.*1449_*1460delinsTTTTTTTTTTTA	NP_001291646.4:n.*1449_*1460delinsTTTTTTTTTTTA
NM_001304718.2:c.*1449_*1460delinsTTTTTTTTTTTA	NP_001291647.1:n.*1449_*1460delinsTTTTTTTTTTTA
NM_000314.8:c.*1449_*1460delinsTTTTTTTTTTTA MANE Select	NP_000305.3:n.*1449_*1460delinsTTTTTTTTTTTA