Canonical Allele Identifier: CA891841301

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952154_87952155delinsCG , CM000672.2:g.87952154_87952155delinsCG	GRCh38
NC_000010.10:g.89711911_89711912delinsCG , CM000672.1:g.89711911_89711912delinsCG	GRCh37
NC_000010.9:g.89701891_89701892delinsCG	NCBI36
NG_007466.2:g.93716_93717delinsCG , LRG_311:g.93716_93717delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.529_530delinsCG	ENSP00000514759.2:p.Tyr177Arg
ENST00000710265.1:c.529_530delinsCG	ENSP00000518161.1:p.Tyr177Arg
ENST00000472832.3:c.529_530delinsCG	ENSP00000483066.2:p.Tyr177Arg
ENST00000688158.2:n.1264_1265delinsCG
ENST00000688922.2:c.*359_*360delinsCG	ENSP00000508742.2:n.*359_*360delinsCG
ENST00000700021.1:c.484_485delinsCG	ENSP00000514757.1:p.Tyr162Arg
ENST00000700022.1:c.493-5699_493-5698delinsCG	ENSP00000514758.1:n.493-5699_493-5698delinsCG
ENST00000700023.1:n.1687_1688delinsCG
ENST00000700024.1:n.1921_1922delinsCG
ENST00000700025.1:n.1298_1299delinsCG
ENST00000700029.1:c.363_364delinsCG
ENST00000706954.1:c.529_530delinsCG	ENSP00000516674.1:p.Tyr177Arg
ENST00000706955.1:c.*564_*565delinsCG	ENSP00000516675.1:n.*564_*565delinsCG
ENST00000686459.1:c.*115_*116delinsCG	ENSP00000508909.1:n.*115_*116delinsCG
ENST00000688158.1:c.*640_*641delinsCG	ENSP00000509254.1:n.*640_*641delinsCG
ENST00000688308.1:c.529_530delinsCG	ENSP00000508752.1:p.Tyr177Arg
ENST00000688922.1:c.450_451delinsCG
ENST00000693560.1:c.1048_1049delinsCG	ENSP00000509861.1:p.Tyr350Arg
ENST00000371953.8:c.529_530delinsCG MANE Select	ENSP00000361021.3:p.Tyr177Arg
ENST00000371953.7:c.529_530delinsCG	ENSP00000361021.3:p.Tyr177Arg
NM_000314.5:c.529_530delinsCG	NP_000305.3:p.Tyr177Arg
NM_000314.6:c.529_530delinsCG	NP_000305.3:p.Tyr177Arg
NM_001304717.2:c.1048_1049delinsCG	NP_001291646.2:p.Tyr350Arg
NM_001304718.1:c.-63_-62delinsCG	NP_001291647.1:n.-63_-62delinsCG
XM_006717926.2:c.484_485delinsCG	XP_006717989.1:p.Tyr162Arg
XM_011539981.1:c.529_530delinsCG	XP_011538283.1:p.Tyr177Arg
XM_011539982.1:c.433_434delinsCG	XP_011538284.1:p.Tyr145Arg
XR_945789.1:n.1400_1401delinsCG
XR_945790.1:n.1517_1518delinsCG
XR_945791.1:n.1205-5699_1205-5698delinsCG
NM_000314.7:c.529_530delinsCG	NP_000305.3:p.Tyr177Arg
NM_001304717.5:c.1048_1049delinsCG	NP_001291646.4:p.Tyr350Arg
NM_001304718.2:c.-63_-62delinsCG	NP_001291647.1:n.-63_-62delinsCG
NM_000314.8:c.529_530delinsCG MANE Select	NP_000305.3:p.Tyr177Arg