Canonical Allele Identifier: CA2530683507

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967897_87967898insA , CM000672.2:g.87967897_87967898insA	GRCh38
NC_000010.10:g.89727654_89727655insA , CM000672.1:g.89727654_89727655insA	GRCh37
NC_000010.9:g.89717634_89717635insA	NCBI36
NG_007466.2:g.109459_109460insA , LRG_311:g.109459_109460insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*2666_*2667insA	ENSP00000518161.1:n.*2666_*2667insA
ENST00000688158.2:n.4372_4373insA
ENST00000706954.1:c.*2425_*2426insA	ENSP00000516674.1:n.*2425_*2426insA
ENST00000706955.1:c.*3672_*3673insA	ENSP00000516675.1:n.*3672_*3673insA
ENST00000688158.1:c.*3748_*3749insA	ENSP00000509254.1:n.*3748_*3749insA
ENST00000693560.1:c.*2425_*2426insA	ENSP00000509861.1:n.*2425_*2426insA
ENST00000371953.8:c.*2425_*2426insA MANE Select	ENSP00000361021.3:n.*2425_*2426insA
ENST00000371953.7:c.*2425_*2426insA	ENSP00000361021.3:n.*2425_*2426insA
NM_000314.5:c.*2425_*2426insA	NP_000305.3:n.*2425_*2426insA
NM_000314.6:c.*2425_*2426insA	NP_000305.3:n.*2425_*2426insA
NM_001304717.2:c.*2425_*2426insA	NP_001291646.2:n.*2425_*2426insA
NM_001304718.1:c.*2425_*2426insA	NP_001291647.1:n.*2425_*2426insA
XM_006717926.2:c.*2425_*2426insA	XP_006717989.1:n.*2425_*2426insA
XM_011539982.1:c.*2425_*2426insA	XP_011538284.1:n.*2425_*2426insA
XR_945791.1:n.4207_4208insA
NM_000314.7:c.*2425_*2426insA	NP_000305.3:n.*2425_*2426insA
NM_001304717.5:c.*2425_*2426insA	NP_001291646.4:n.*2425_*2426insA
NM_001304718.2:c.*2425_*2426insA	NP_001291647.1:n.*2425_*2426insA
NM_000314.8:c.*2425_*2426insA MANE Select	NP_000305.3:n.*2425_*2426insA