Canonical Allele Identifier: CA891841592

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965351_87965352delinsTA , CM000672.2:g.87965351_87965352delinsTA	GRCh38
NC_000010.10:g.89725108_89725109delinsTA , CM000672.1:g.89725108_89725109delinsTA	GRCh37
NC_000010.9:g.89715088_89715089delinsTA	NCBI36
NG_007466.2:g.106913_106914delinsTA , LRG_311:g.106913_106914delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1184_1185delinsTA	ENSP00000514759.2:p.Ser395Leu
ENST00000710265.1:c.*120_*121delinsTA	ENSP00000518161.1:n.*120_*121delinsTA
ENST00000688158.2:n.1826_1827delinsTA
ENST00000688922.2:c.*921_*922delinsTA	ENSP00000508742.2:n.*921_*922delinsTA
ENST00000700021.1:c.1046_1047delinsTA	ENSP00000514757.1:p.Ser349Leu
ENST00000700022.1:c.*430_*431delinsTA	ENSP00000514758.1:n.*430_*431delinsTA
ENST00000700023.1:n.2249_2250delinsTA
ENST00000700024.1:n.2483_2484delinsTA
ENST00000706954.1:c.1091_1092delinsTA	ENSP00000516674.1:p.Ser364Leu
ENST00000706955.1:c.*1126_*1127delinsTA	ENSP00000516675.1:n.*1126_*1127delinsTA
ENST00000686459.1:c.*677_*678delinsTA	ENSP00000508909.1:n.*677_*678delinsTA
ENST00000688158.1:c.*1202_*1203delinsTA	ENSP00000509254.1:n.*1202_*1203delinsTA
ENST00000688308.1:c.1091_1092delinsTA	ENSP00000508752.1:p.Ser364Leu
ENST00000688922.1:c.1012_1013delinsTA
ENST00000693560.1:c.1610_1611delinsTA	ENSP00000509861.1:p.Ser537Leu
ENST00000371953.8:c.1091_1092delinsTA MANE Select	ENSP00000361021.3:p.Ser364Leu
ENST00000371953.7:c.1091_1092delinsTA	ENSP00000361021.3:p.Ser364Leu
NM_000314.5:c.1091_1092delinsTA	NP_000305.3:p.Ser364Leu
NM_000314.6:c.1091_1092delinsTA	NP_000305.3:p.Ser364Leu
NM_001304717.2:c.1610_1611delinsTA	NP_001291646.2:p.Ser537Leu
NM_001304718.1:c.500_501delinsTA	NP_001291647.1:p.Ser167Leu
XM_006717926.2:c.1046_1047delinsTA	XP_006717989.1:p.Ser349Leu
XM_011539982.1:c.995_996delinsTA	XP_011538284.1:p.Ser332Leu
XR_945791.1:n.1661_1662delinsTA
NM_000314.7:c.1091_1092delinsTA	NP_000305.3:p.Ser364Leu
NM_001304717.5:c.1610_1611delinsTA	NP_001291646.4:p.Ser537Leu
NM_001304718.2:c.500_501delinsTA	NP_001291647.1:p.Ser167Leu
NM_000314.8:c.1091_1092delinsTA MANE Select	NP_000305.3:p.Ser364Leu