Canonical Allele Identifier: CA211453334

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87864104del , CM000672.2:g.87864104del	GRCh38
NC_000010.10:g.89623861del , CM000672.1:g.89623861del	GRCh37
NC_000010.9:g.89613841del	NCBI36
NG_033079.1:g.4334del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.-366del	ENSP00000514759.2:n.-366del
ENST00000710265.1:c.-366del	ENSP00000518161.1:n.-366del
ENST00000700021.1:c.-366del	ENSP00000514757.1:n.-366del
ENST00000700022.1:c.-366del	ENSP00000514758.1:n.-366del
ENST00000706954.1:c.-16-350del	ENSP00000516674.1:n.-16-350del
ENST00000706955.1:c.-366del	ENSP00000516675.1:n.-366del
ENST00000688158.1:c.-366del	ENSP00000509254.1:n.-366del
ENST00000688308.1:c.-16-350del	ENSP00000508752.1:n.-16-350del
ENST00000693560.1:c.155-1del	ENSP00000509861.1:n.155-1del
ENST00000371953.8:c.-366del MANE Select	ENSP00000361021.3:n.-366del
ENST00000371953.7:c.-366del	ENSP00000361021.3:n.-366del
ENST00000610634.1:c.-468del	ENSP00000477517.1:n.-468del
XM_006717926.2:c.-366del	XP_006717989.1:n.-366del
XM_011539981.1:c.-366del	XP_011538283.1:n.-366del
XR_945789.1:n.347del
XR_945790.1:n.347del
XR_945791.1:n.347del
NM_000314.8:c.-366del MANE Select	NP_000305.3:n.-366del