Canonical Allele Identifier: CA891840352

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925526_87925527delinsGT , CM000672.2:g.87925526_87925527delinsGT	GRCh38
NC_000010.10:g.89685283_89685284delinsGT , CM000672.1:g.89685283_89685284delinsGT	GRCh37
NC_000010.9:g.89675263_89675264delinsGT	NCBI36
NG_007466.2:g.67088_67089delinsGT , LRG_311:g.67088_67089delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.178_179delinsGT	ENSP00000514759.2:p.Lys60Val
ENST00000710265.1:c.178_179delinsGT	ENSP00000518161.1:p.Lys60Val
ENST00000472832.3:c.178_179delinsGT	ENSP00000483066.2:p.Lys60Val
ENST00000688158.2:n.913_914delinsGT
ENST00000688922.2:c.178_179delinsGT	ENSP00000508742.2:p.Lys60Val
ENST00000700021.1:c.165-5520_165-5519delinsGT	ENSP00000514757.1:n.165-5520_165-5519delinsGT
ENST00000700022.1:c.178_179delinsGT	ENSP00000514758.1:p.Lys60Val
ENST00000700029.1:c.12_13delinsGT
ENST00000706954.1:c.178_179delinsGT	ENSP00000516674.1:p.Lys60Val
ENST00000706955.1:c.*213_*214delinsGT	ENSP00000516675.1:n.*213_*214delinsGT
ENST00000686459.1:c.178_179delinsGT	ENSP00000508909.1:p.Lys60Val
ENST00000688158.1:c.*289_*290delinsGT	ENSP00000509254.1:n.*289_*290delinsGT
ENST00000688308.1:c.178_179delinsGT	ENSP00000508752.1:p.Lys60Val
ENST00000688922.1:c.47_48delinsGT
ENST00000693560.1:c.697_698delinsGT	ENSP00000509861.1:p.Lys233Val
ENST00000371953.8:c.178_179delinsGT MANE Select	ENSP00000361021.3:p.Lys60Val
ENST00000371953.7:c.178_179delinsGT	ENSP00000361021.3:p.Lys60Val
ENST00000498703.1:n.4_5delinsGT
ENST00000610634.1:c.76_77delinsGT	ENSP00000477517.1:p.Lys26Val
NM_000314.5:c.178_179delinsGT	NP_000305.3:p.Lys60Val
NM_000314.6:c.178_179delinsGT	NP_000305.3:p.Lys60Val
NM_001304717.2:c.697_698delinsGT	NP_001291646.2:p.Lys233Val
NM_001304718.1:c.-541-5520_-541-5519delinsGT	NP_001291647.1:n.-541-5520_-541-5519delinsGT
XM_006717926.2:c.165-5520_165-5519delinsGT	XP_006717989.1:n.165-5520_165-5519delinsGT
XM_011539981.1:c.178_179delinsGT	XP_011538283.1:p.Lys60Val
XM_011539982.1:c.82_83delinsGT	XP_011538284.1:p.Lys28Val
XR_945789.1:n.890_891delinsGT
XR_945790.1:n.890_891delinsGT
XR_945791.1:n.890_891delinsGT
NM_000314.7:c.178_179delinsGT	NP_000305.3:p.Lys60Val
NM_001304717.5:c.697_698delinsGT	NP_001291646.4:p.Lys233Val
NM_001304718.2:c.-541-5520_-541-5519delinsGT	NP_001291647.1:n.-541-5520_-541-5519delinsGT
NM_000314.8:c.178_179delinsGT MANE Select	NP_000305.3:p.Lys60Val