Canonical Allele Identifier: CA1926177587

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967976_87967980delinsCTTTA , CM000672.2:g.87967976_87967980delinsCTTTA	GRCh38
NC_000010.10:g.89727733_89727737delinsCTTTA , CM000672.1:g.89727733_89727737delinsCTTTA	GRCh37
NC_000010.9:g.89717713_89717717delinsCTTTA	NCBI36
NG_007466.2:g.109538_109542delinsCTTTA , LRG_311:g.109538_109542delinsCTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*2745_*2749delinsCTTTA	ENSP00000518161.1:n.*2745_*2749delinsCTTTA
ENST00000688158.2:n.4451_4455delinsCTTTA
ENST00000706954.1:c.*2504_*2508delinsCTTTA	ENSP00000516674.1:n.*2504_*2508delinsCTTTA
ENST00000706955.1:c.*3751_*3755delinsCTTTA	ENSP00000516675.1:n.*3751_*3755delinsCTTTA
ENST00000688158.1:c.*3827_*3831delinsCTTTA	ENSP00000509254.1:n.*3827_*3831delinsCTTTA
ENST00000693560.1:c.*2504_*2508delinsCTTTA	ENSP00000509861.1:n.*2504_*2508delinsCTTTA
ENST00000371953.8:c.*2504_*2508delinsCTTTA MANE Select	ENSP00000361021.3:n.*2504_*2508delinsCTTTA
ENST00000371953.7:c.*2504_*2508delinsCTTTA	ENSP00000361021.3:n.*2504_*2508delinsCTTTA
NM_000314.5:c.*2504_*2508delinsCTTTA	NP_000305.3:n.*2504_*2508delinsCTTTA
NM_000314.6:c.*2504_*2508delinsCTTTA	NP_000305.3:n.*2504_*2508delinsCTTTA
NM_001304717.2:c.*2504_*2508delinsCTTTA	NP_001291646.2:n.*2504_*2508delinsCTTTA
NM_001304718.1:c.*2504_*2508delinsCTTTA	NP_001291647.1:n.*2504_*2508delinsCTTTA
XM_006717926.2:c.*2504_*2508delinsCTTTA	XP_006717989.1:n.*2504_*2508delinsCTTTA
XM_011539982.1:c.*2504_*2508delinsCTTTA	XP_011538284.1:n.*2504_*2508delinsCTTTA
XR_945791.1:n.4286_4290delinsCTTTA
NM_000314.7:c.*2504_*2508delinsCTTTA	NP_000305.3:n.*2504_*2508delinsCTTTA
NM_001304717.5:c.*2504_*2508delinsCTTTA	NP_001291646.4:n.*2504_*2508delinsCTTTA
NM_001304718.2:c.*2504_*2508delinsCTTTA	NP_001291647.1:n.*2504_*2508delinsCTTTA
NM_000314.8:c.*2504_*2508delinsCTTTA MANE Select	NP_000305.3:n.*2504_*2508delinsCTTTA