Canonical Allele Identifier: CA1926176834

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967506_87967511delinsACTATT , CM000672.2:g.87967506_87967511delinsACTATT	GRCh38
NC_000010.10:g.89727263_89727268delinsACTATT , CM000672.1:g.89727263_89727268delinsACTATT	GRCh37
NC_000010.9:g.89717243_89717248delinsACTATT	NCBI36
NG_007466.2:g.109068_109073delinsACTATT , LRG_311:g.109068_109073delinsACTATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*2275_*2280delinsACTATT	ENSP00000518161.1:n.*2275_*2280delinsACTATT
ENST00000688158.2:n.3981_3986delinsACTATT
ENST00000706954.1:c.*2034_*2039delinsACTATT	ENSP00000516674.1:n.*2034_*2039delinsACTATT
ENST00000706955.1:c.*3281_*3286delinsACTATT	ENSP00000516675.1:n.*3281_*3286delinsACTATT
ENST00000688158.1:c.*3357_*3362delinsACTATT	ENSP00000509254.1:n.*3357_*3362delinsACTATT
ENST00000693560.1:c.*2034_*2039delinsACTATT	ENSP00000509861.1:n.*2034_*2039delinsACTATT
ENST00000371953.8:c.*2034_*2039delinsACTATT MANE Select	ENSP00000361021.3:n.*2034_*2039delinsACTATT
ENST00000371953.7:c.*2034_*2039delinsACTATT	ENSP00000361021.3:n.*2034_*2039delinsACTATT
NM_000314.5:c.*2034_*2039delinsACTATT	NP_000305.3:n.*2034_*2039delinsACTATT
NM_000314.6:c.*2034_*2039delinsACTATT	NP_000305.3:n.*2034_*2039delinsACTATT
NM_001304717.2:c.*2034_*2039delinsACTATT	NP_001291646.2:n.*2034_*2039delinsACTATT
NM_001304718.1:c.*2034_*2039delinsACTATT	NP_001291647.1:n.*2034_*2039delinsACTATT
XM_006717926.2:c.*2034_*2039delinsACTATT	XP_006717989.1:n.*2034_*2039delinsACTATT
XM_011539982.1:c.*2034_*2039delinsACTATT	XP_011538284.1:n.*2034_*2039delinsACTATT
XR_945791.1:n.3816_3821delinsACTATT
NM_000314.7:c.*2034_*2039delinsACTATT	NP_000305.3:n.*2034_*2039delinsACTATT
NM_001304717.5:c.*2034_*2039delinsACTATT	NP_001291646.4:n.*2034_*2039delinsACTATT
NM_001304718.2:c.*2034_*2039delinsACTATT	NP_001291647.1:n.*2034_*2039delinsACTATT
NM_000314.8:c.*2034_*2039delinsACTATT MANE Select	NP_000305.3:n.*2034_*2039delinsACTATT