Canonical Allele Identifier: CA669574845

Gene: PTEN

Linked Data

• dbSNP Id: rs1168500453
• MyVariant Identifiers: chr10:g.87967386_87967389del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967390_87967393del , CM000672.2:g.87967390_87967393del	GRCh38
NC_000010.10:g.89727147_89727150del , CM000672.1:g.89727147_89727150del	GRCh37
NC_000010.9:g.89717127_89717130del	NCBI36
NG_007466.2:g.108952_108955del , LRG_311:g.108952_108955del

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*2159_*2162del	ENSP00000518161.1:n.*2159_*2162del
ENST00000688158.2:n.3865_3868del
ENST00000706954.1:c.*1918_*1921del	ENSP00000516674.1:n.*1918_*1921del
ENST00000706955.1:c.*3165_*3168del	ENSP00000516675.1:n.*3165_*3168del
ENST00000688158.1:c.*3241_*3244del	ENSP00000509254.1:n.*3241_*3244del
ENST00000693560.1:c.*1918_*1921del	ENSP00000509861.1:n.*1918_*1921del
ENST00000371953.8:c.*1918_*1921del MANE Select	ENSP00000361021.3:n.*1918_*1921del
ENST00000371953.7:c.*1918_*1921del	ENSP00000361021.3:n.*1918_*1921del
NM_000314.5:c.*1918_*1921del	NP_000305.3:n.*1918_*1921del
NM_000314.6:c.*1918_*1921del	NP_000305.3:n.*1918_*1921del
NM_001304717.2:c.*1918_*1921del	NP_001291646.2:n.*1918_*1921del
NM_001304718.1:c.*1918_*1921del	NP_001291647.1:n.*1918_*1921del
XM_006717926.2:c.*1918_*1921del	XP_006717989.1:n.*1918_*1921del
XM_011539982.1:c.*1918_*1921del	XP_011538284.1:n.*1918_*1921del
XR_945791.1:n.3700_3703del
NM_000314.7:c.*1918_*1921del	NP_000305.3:n.*1918_*1921del
NM_001304717.5:c.*1918_*1921del	NP_001291646.4:n.*1918_*1921del
NM_001304718.2:c.*1918_*1921del	NP_001291647.1:n.*1918_*1921del
NM_000314.8:c.*1918_*1921del MANE Select	NP_000305.3:n.*1918_*1921del