Canonical Allele Identifier: CA891837844

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965398_87965399delinsGA , CM000672.2:g.87965398_87965399delinsGA	GRCh38
NC_000010.10:g.89725155_89725156delinsGA , CM000672.1:g.89725155_89725156delinsGA	GRCh37
NC_000010.9:g.89715135_89715136delinsGA	NCBI36
NG_007466.2:g.106960_106961delinsGA , LRG_311:g.106960_106961delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1231_1232delinsGA	ENSP00000514759.2:p.Ser411Asp
ENST00000710265.1:c.*167_*168delinsGA	ENSP00000518161.1:n.*167_*168delinsGA
ENST00000688158.2:n.1873_1874delinsGA
ENST00000688922.2:c.*968_*969delinsGA	ENSP00000508742.2:n.*968_*969delinsGA
ENST00000700021.1:c.1093_1094delinsGA	ENSP00000514757.1:p.Ser365Asp
ENST00000700022.1:c.*477_*478delinsGA	ENSP00000514758.1:n.*477_*478delinsGA
ENST00000700023.1:n.2296_2297delinsGA
ENST00000700024.1:n.2530_2531delinsGA
ENST00000706954.1:c.1138_1139delinsGA	ENSP00000516674.1:p.Ser380Asp
ENST00000706955.1:c.*1173_*1174delinsGA	ENSP00000516675.1:n.*1173_*1174delinsGA
ENST00000686459.1:c.*724_*725delinsGA	ENSP00000508909.1:n.*724_*725delinsGA
ENST00000688158.1:c.*1249_*1250delinsGA	ENSP00000509254.1:n.*1249_*1250delinsGA
ENST00000688308.1:c.1138_1139delinsGA	ENSP00000508752.1:p.Ser380Asp
ENST00000688922.1:c.1059_1060delinsGA
ENST00000693560.1:c.1657_1658delinsGA	ENSP00000509861.1:p.Ser553Asp
ENST00000371953.8:c.1138_1139delinsGA MANE Select	ENSP00000361021.3:p.Ser380Asp
ENST00000371953.7:c.1138_1139delinsGA	ENSP00000361021.3:p.Ser380Asp
NM_000314.5:c.1138_1139delinsGA	NP_000305.3:p.Ser380Asp
NM_000314.6:c.1138_1139delinsGA	NP_000305.3:p.Ser380Asp
NM_001304717.2:c.1657_1658delinsGA	NP_001291646.2:p.Ser553Asp
NM_001304718.1:c.547_548delinsGA	NP_001291647.1:p.Ser183Asp
XM_006717926.2:c.1093_1094delinsGA	XP_006717989.1:p.Ser365Asp
XM_011539982.1:c.1042_1043delinsGA	XP_011538284.1:p.Ser348Asp
XR_945791.1:n.1708_1709delinsGA
NM_000314.7:c.1138_1139delinsGA	NP_000305.3:p.Ser380Asp
NM_001304717.5:c.1657_1658delinsGA	NP_001291646.4:p.Ser553Asp
NM_001304718.2:c.547_548delinsGA	NP_001291647.1:p.Ser183Asp
NM_000314.8:c.1138_1139delinsGA MANE Select	NP_000305.3:p.Ser380Asp