Canonical Allele Identifier: CA2788898661

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967512dup , CM000672.2:g.87967512dup	GRCh38
NC_000010.10:g.89727269dup , CM000672.1:g.89727269dup	GRCh37
NC_000010.9:g.89717249dup	NCBI36
NG_007466.2:g.109074dup , LRG_311:g.109074dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*2281dup	ENSP00000518161.1:n.*2281dup
ENST00000688158.2:n.3987dup
ENST00000706954.1:c.*2040dup	ENSP00000516674.1:n.*2040dup
ENST00000706955.1:c.*3287dup	ENSP00000516675.1:n.*3287dup
ENST00000688158.1:c.*3363dup	ENSP00000509254.1:n.*3363dup
ENST00000693560.1:c.*2040dup	ENSP00000509861.1:n.*2040dup
ENST00000371953.8:c.*2040dup MANE Select	ENSP00000361021.3:n.*2040dup
ENST00000371953.7:c.*2040dup	ENSP00000361021.3:n.*2040dup
NM_000314.5:c.*2040dup	NP_000305.3:n.*2040dup
NM_000314.6:c.*2040dup	NP_000305.3:n.*2040dup
NM_001304717.2:c.*2040dup	NP_001291646.2:n.*2040dup
NM_001304718.1:c.*2040dup	NP_001291647.1:n.*2040dup
XM_006717926.2:c.*2040dup	XP_006717989.1:n.*2040dup
XM_011539982.1:c.*2040dup	XP_011538284.1:n.*2040dup
XR_945791.1:n.3822dup
NM_000314.7:c.*2040dup	NP_000305.3:n.*2040dup
NM_001304717.5:c.*2040dup	NP_001291646.4:n.*2040dup
NM_001304718.2:c.*2040dup	NP_001291647.1:n.*2040dup
NM_000314.8:c.*2040dup MANE Select	NP_000305.3:n.*2040dup