Canonical Allele Identifier: CA891837439

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965351_87965352delinsAA , CM000672.2:g.87965351_87965352delinsAA	GRCh38
NC_000010.10:g.89725108_89725109delinsAA , CM000672.1:g.89725108_89725109delinsAA	GRCh37
NC_000010.9:g.89715088_89715089delinsAA	NCBI36
NG_007466.2:g.106913_106914delinsAA , LRG_311:g.106913_106914delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1184_1185delinsAA	ENSP00000514759.2:p.Ser395Ter
ENST00000710265.1:c.*120_*121delinsAA	ENSP00000518161.1:n.*120_*121delinsAA
ENST00000688158.2:n.1826_1827delinsAA
ENST00000688922.2:c.*921_*922delinsAA	ENSP00000508742.2:n.*921_*922delinsAA
ENST00000700021.1:c.1046_1047delinsAA	ENSP00000514757.1:p.Ser349Ter
ENST00000700022.1:c.*430_*431delinsAA	ENSP00000514758.1:n.*430_*431delinsAA
ENST00000700023.1:n.2249_2250delinsAA
ENST00000700024.1:n.2483_2484delinsAA
ENST00000706954.1:c.1091_1092delinsAA	ENSP00000516674.1:p.Ser364Ter
ENST00000706955.1:c.*1126_*1127delinsAA	ENSP00000516675.1:n.*1126_*1127delinsAA
ENST00000686459.1:c.*677_*678delinsAA	ENSP00000508909.1:n.*677_*678delinsAA
ENST00000688158.1:c.*1202_*1203delinsAA	ENSP00000509254.1:n.*1202_*1203delinsAA
ENST00000688308.1:c.1091_1092delinsAA	ENSP00000508752.1:p.Ser364Ter
ENST00000688922.1:c.1012_1013delinsAA
ENST00000693560.1:c.1610_1611delinsAA	ENSP00000509861.1:p.Ser537Ter
ENST00000371953.8:c.1091_1092delinsAA MANE Select	ENSP00000361021.3:p.Ser364Ter
ENST00000371953.7:c.1091_1092delinsAA	ENSP00000361021.3:p.Ser364Ter
NM_000314.5:c.1091_1092delinsAA	NP_000305.3:p.Ser364Ter
NM_000314.6:c.1091_1092delinsAA	NP_000305.3:p.Ser364Ter
NM_001304717.2:c.1610_1611delinsAA	NP_001291646.2:p.Ser537Ter
NM_001304718.1:c.500_501delinsAA	NP_001291647.1:p.Ser167Ter
XM_006717926.2:c.1046_1047delinsAA	XP_006717989.1:p.Ser349Ter
XM_011539982.1:c.995_996delinsAA	XP_011538284.1:p.Ser332Ter
XR_945791.1:n.1661_1662delinsAA
NM_000314.7:c.1091_1092delinsAA	NP_000305.3:p.Ser364Ter
NM_001304717.5:c.1610_1611delinsAA	NP_001291646.4:p.Ser537Ter
NM_001304718.2:c.500_501delinsAA	NP_001291647.1:p.Ser167Ter
NM_000314.8:c.1091_1092delinsAA MANE Select	NP_000305.3:p.Ser364Ter