Canonical Allele Identifier: CA1926176083

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967013_87967014delinsCA , CM000672.2:g.87967013_87967014delinsCA	GRCh38
NC_000010.10:g.89726770_89726771delinsCA , CM000672.1:g.89726770_89726771delinsCA	GRCh37
NC_000010.9:g.89716750_89716751delinsCA	NCBI36
NG_007466.2:g.108575_108576delinsCA , LRG_311:g.108575_108576delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*1782_*1783delinsCA	ENSP00000518161.1:n.*1782_*1783delinsCA
ENST00000688158.2:n.3488_3489delinsCA
ENST00000706954.1:c.*1541_*1542delinsCA	ENSP00000516674.1:n.*1541_*1542delinsCA
ENST00000706955.1:c.*2788_*2789delinsCA	ENSP00000516675.1:n.*2788_*2789delinsCA
ENST00000688158.1:c.*2864_*2865delinsCA	ENSP00000509254.1:n.*2864_*2865delinsCA
ENST00000693560.1:c.*1541_*1542delinsCA	ENSP00000509861.1:n.*1541_*1542delinsCA
ENST00000371953.8:c.*1541_*1542delinsCA MANE Select	ENSP00000361021.3:n.*1541_*1542delinsCA
ENST00000371953.7:c.*1541_*1542delinsCA	ENSP00000361021.3:n.*1541_*1542delinsCA
NM_000314.5:c.*1541_*1542delinsCA	NP_000305.3:n.*1541_*1542delinsCA
NM_000314.6:c.*1541_*1542delinsCA	NP_000305.3:n.*1541_*1542delinsCA
NM_001304717.2:c.*1541_*1542delinsCA	NP_001291646.2:n.*1541_*1542delinsCA
NM_001304718.1:c.*1541_*1542delinsCA	NP_001291647.1:n.*1541_*1542delinsCA
XM_006717926.2:c.*1541_*1542delinsCA	XP_006717989.1:n.*1541_*1542delinsCA
XM_011539982.1:c.*1541_*1542delinsCA	XP_011538284.1:n.*1541_*1542delinsCA
XR_945791.1:n.3323_3324delinsCA
NM_000314.7:c.*1541_*1542delinsCA	NP_000305.3:n.*1541_*1542delinsCA
NM_001304717.5:c.*1541_*1542delinsCA	NP_001291646.4:n.*1541_*1542delinsCA
NM_001304718.2:c.*1541_*1542delinsCA	NP_001291647.1:n.*1541_*1542delinsCA
NM_000314.8:c.*1541_*1542delinsCA MANE Select	NP_000305.3:n.*1541_*1542delinsCA