Canonical Allele Identifier: CA1926175680

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966899_87966900delinsAG , CM000672.2:g.87966899_87966900delinsAG	GRCh38
NC_000010.10:g.89726656_89726657delinsAG , CM000672.1:g.89726656_89726657delinsAG	GRCh37
NC_000010.9:g.89716636_89716637delinsAG	NCBI36
NG_007466.2:g.108461_108462delinsAG , LRG_311:g.108461_108462delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*1668_*1669delinsAG	ENSP00000518161.1:n.*1668_*1669delinsAG
ENST00000688158.2:n.3374_3375delinsAG
ENST00000706954.1:c.*1427_*1428delinsAG	ENSP00000516674.1:n.*1427_*1428delinsAG
ENST00000706955.1:c.*2674_*2675delinsAG	ENSP00000516675.1:n.*2674_*2675delinsAG
ENST00000688158.1:c.*2750_*2751delinsAG	ENSP00000509254.1:n.*2750_*2751delinsAG
ENST00000693560.1:c.*1427_*1428delinsAG	ENSP00000509861.1:n.*1427_*1428delinsAG
ENST00000371953.8:c.*1427_*1428delinsAG MANE Select	ENSP00000361021.3:n.*1427_*1428delinsAG
ENST00000371953.7:c.*1427_*1428delinsAG	ENSP00000361021.3:n.*1427_*1428delinsAG
NM_000314.5:c.*1427_*1428delinsAG	NP_000305.3:n.*1427_*1428delinsAG
NM_000314.6:c.*1427_*1428delinsAG	NP_000305.3:n.*1427_*1428delinsAG
NM_001304717.2:c.*1427_*1428delinsAG	NP_001291646.2:n.*1427_*1428delinsAG
NM_001304718.1:c.*1427_*1428delinsAG	NP_001291647.1:n.*1427_*1428delinsAG
XM_006717926.2:c.*1427_*1428delinsAG	XP_006717989.1:n.*1427_*1428delinsAG
XM_011539982.1:c.*1427_*1428delinsAG	XP_011538284.1:n.*1427_*1428delinsAG
XR_945791.1:n.3209_3210delinsAG
NM_000314.7:c.*1427_*1428delinsAG	NP_000305.3:n.*1427_*1428delinsAG
NM_001304717.5:c.*1427_*1428delinsAG	NP_001291646.4:n.*1427_*1428delinsAG
NM_001304718.2:c.*1427_*1428delinsAG	NP_001291647.1:n.*1427_*1428delinsAG
NM_000314.8:c.*1427_*1428delinsAG MANE Select	NP_000305.3:n.*1427_*1428delinsAG