Canonical Allele Identifier: CA891837513

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965359_87965361delinsATG , CM000672.2:g.87965359_87965361delinsATG	GRCh38
NC_000010.10:g.89725116_89725118delinsATG , CM000672.1:g.89725116_89725118delinsATG	GRCh37
NC_000010.9:g.89715096_89715098delinsATG	NCBI36
NG_007466.2:g.106921_106923delinsATG , LRG_311:g.106921_106923delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1192_1194delinsATG	ENSP00000514759.2:p.Pro398Met
ENST00000710265.1:c.*128_*130delinsATG	ENSP00000518161.1:n.*128_*130delinsATG
ENST00000688158.2:n.1834_1836delinsATG
ENST00000688922.2:c.*929_*931delinsATG	ENSP00000508742.2:n.*929_*931delinsATG
ENST00000700021.1:c.1054_1056delinsATG	ENSP00000514757.1:p.Pro352Met
ENST00000700022.1:c.*438_*440delinsATG	ENSP00000514758.1:n.*438_*440delinsATG
ENST00000700023.1:n.2257_2259delinsATG
ENST00000700024.1:n.2491_2493delinsATG
ENST00000706954.1:c.1099_1101delinsATG	ENSP00000516674.1:p.Pro367Met
ENST00000706955.1:c.*1134_*1136delinsATG	ENSP00000516675.1:n.*1134_*1136delinsATG
ENST00000686459.1:c.*685_*687delinsATG	ENSP00000508909.1:n.*685_*687delinsATG
ENST00000688158.1:c.*1210_*1212delinsATG	ENSP00000509254.1:n.*1210_*1212delinsATG
ENST00000688308.1:c.1099_1101delinsATG	ENSP00000508752.1:p.Pro367Met
ENST00000688922.1:c.1020_1022delinsATG
ENST00000693560.1:c.1618_1620delinsATG	ENSP00000509861.1:p.Pro540Met
ENST00000371953.8:c.1099_1101delinsATG MANE Select	ENSP00000361021.3:p.Pro367Met
ENST00000371953.7:c.1099_1101delinsATG	ENSP00000361021.3:p.Pro367Met
NM_000314.5:c.1099_1101delinsATG	NP_000305.3:p.Pro367Met
NM_000314.6:c.1099_1101delinsATG	NP_000305.3:p.Pro367Met
NM_001304717.2:c.1618_1620delinsATG	NP_001291646.2:p.Pro540Met
NM_001304718.1:c.508_510delinsATG	NP_001291647.1:p.Pro170Met
XM_006717926.2:c.1054_1056delinsATG	XP_006717989.1:p.Pro352Met
XM_011539982.1:c.1003_1005delinsATG	XP_011538284.1:p.Pro335Met
XR_945791.1:n.1669_1671delinsATG
NM_000314.7:c.1099_1101delinsATG	NP_000305.3:p.Pro367Met
NM_001304717.5:c.1618_1620delinsATG	NP_001291646.4:p.Pro540Met
NM_001304718.2:c.508_510delinsATG	NP_001291647.1:p.Pro170Met
NM_000314.8:c.1099_1101delinsATG MANE Select	NP_000305.3:p.Pro367Met