Canonical Allele Identifier: CA891837820

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965393_87965394delinsTG , CM000672.2:g.87965393_87965394delinsTG	GRCh38
NC_000010.10:g.89725150_89725151delinsTG , CM000672.1:g.89725150_89725151delinsTG	GRCh37
NC_000010.9:g.89715130_89715131delinsTG	NCBI36
NG_007466.2:g.106955_106956delinsTG , LRG_311:g.106955_106956delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1226_1227delinsTG	ENSP00000514759.2:p.Arg409Met
ENST00000710265.1:c.*162_*163delinsTG	ENSP00000518161.1:n.*162_*163delinsTG
ENST00000688158.2:n.1868_1869delinsTG
ENST00000688922.2:c.*963_*964delinsTG	ENSP00000508742.2:n.*963_*964delinsTG
ENST00000700021.1:c.1088_1089delinsTG	ENSP00000514757.1:p.Arg363Met
ENST00000700022.1:c.*472_*473delinsTG	ENSP00000514758.1:n.*472_*473delinsTG
ENST00000700023.1:n.2291_2292delinsTG
ENST00000700024.1:n.2525_2526delinsTG
ENST00000706954.1:c.1133_1134delinsTG	ENSP00000516674.1:p.Arg378Met
ENST00000706955.1:c.*1168_*1169delinsTG	ENSP00000516675.1:n.*1168_*1169delinsTG
ENST00000686459.1:c.*719_*720delinsTG	ENSP00000508909.1:n.*719_*720delinsTG
ENST00000688158.1:c.*1244_*1245delinsTG	ENSP00000509254.1:n.*1244_*1245delinsTG
ENST00000688308.1:c.1133_1134delinsTG	ENSP00000508752.1:p.Arg378Met
ENST00000688922.1:c.1054_1055delinsTG
ENST00000693560.1:c.1652_1653delinsTG	ENSP00000509861.1:p.Arg551Met
ENST00000371953.8:c.1133_1134delinsTG MANE Select	ENSP00000361021.3:p.Arg378Met
ENST00000371953.7:c.1133_1134delinsTG	ENSP00000361021.3:p.Arg378Met
NM_000314.5:c.1133_1134delinsTG	NP_000305.3:p.Arg378Met
NM_000314.6:c.1133_1134delinsTG	NP_000305.3:p.Arg378Met
NM_001304717.2:c.1652_1653delinsTG	NP_001291646.2:p.Arg551Met
NM_001304718.1:c.542_543delinsTG	NP_001291647.1:p.Arg181Met
XM_006717926.2:c.1088_1089delinsTG	XP_006717989.1:p.Arg363Met
XM_011539982.1:c.1037_1038delinsTG	XP_011538284.1:p.Arg346Met
XR_945791.1:n.1703_1704delinsTG
NM_000314.7:c.1133_1134delinsTG	NP_000305.3:p.Arg378Met
NM_001304717.5:c.1652_1653delinsTG	NP_001291646.4:p.Arg551Met
NM_001304718.2:c.542_543delinsTG	NP_001291647.1:p.Arg181Met
NM_000314.8:c.1133_1134delinsTG MANE Select	NP_000305.3:p.Arg378Met