Canonical Allele Identifier: CA891838792

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952154_87952155delinsGC , CM000672.2:g.87952154_87952155delinsGC	GRCh38
NC_000010.10:g.89711911_89711912delinsGC , CM000672.1:g.89711911_89711912delinsGC	GRCh37
NC_000010.9:g.89701891_89701892delinsGC	NCBI36
NG_007466.2:g.93716_93717delinsGC , LRG_311:g.93716_93717delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.529_530delinsGC	ENSP00000514759.2:p.Tyr177Ala
ENST00000710265.1:c.529_530delinsGC	ENSP00000518161.1:p.Tyr177Ala
ENST00000472832.3:c.529_530delinsGC	ENSP00000483066.2:p.Tyr177Ala
ENST00000688158.2:n.1264_1265delinsGC
ENST00000688922.2:c.*359_*360delinsGC	ENSP00000508742.2:n.*359_*360delinsGC
ENST00000700021.1:c.484_485delinsGC	ENSP00000514757.1:p.Tyr162Ala
ENST00000700022.1:c.493-5699_493-5698delinsGC	ENSP00000514758.1:n.493-5699_493-5698delinsGC
ENST00000700023.1:n.1687_1688delinsGC
ENST00000700024.1:n.1921_1922delinsGC
ENST00000700025.1:n.1298_1299delinsGC
ENST00000700029.1:c.363_364delinsGC
ENST00000706954.1:c.529_530delinsGC	ENSP00000516674.1:p.Tyr177Ala
ENST00000706955.1:c.*564_*565delinsGC	ENSP00000516675.1:n.*564_*565delinsGC
ENST00000686459.1:c.*115_*116delinsGC	ENSP00000508909.1:n.*115_*116delinsGC
ENST00000688158.1:c.*640_*641delinsGC	ENSP00000509254.1:n.*640_*641delinsGC
ENST00000688308.1:c.529_530delinsGC	ENSP00000508752.1:p.Tyr177Ala
ENST00000688922.1:c.450_451delinsGC
ENST00000693560.1:c.1048_1049delinsGC	ENSP00000509861.1:p.Tyr350Ala
ENST00000371953.8:c.529_530delinsGC MANE Select	ENSP00000361021.3:p.Tyr177Ala
ENST00000371953.7:c.529_530delinsGC	ENSP00000361021.3:p.Tyr177Ala
NM_000314.5:c.529_530delinsGC	NP_000305.3:p.Tyr177Ala
NM_000314.6:c.529_530delinsGC	NP_000305.3:p.Tyr177Ala
NM_001304717.2:c.1048_1049delinsGC	NP_001291646.2:p.Tyr350Ala
NM_001304718.1:c.-63_-62delinsGC	NP_001291647.1:n.-63_-62delinsGC
XM_006717926.2:c.484_485delinsGC	XP_006717989.1:p.Tyr162Ala
XM_011539981.1:c.529_530delinsGC	XP_011538283.1:p.Tyr177Ala
XM_011539982.1:c.433_434delinsGC	XP_011538284.1:p.Tyr145Ala
XR_945789.1:n.1400_1401delinsGC
XR_945790.1:n.1517_1518delinsGC
XR_945791.1:n.1205-5699_1205-5698delinsGC
NM_000314.7:c.529_530delinsGC	NP_000305.3:p.Tyr177Ala
NM_001304717.5:c.1048_1049delinsGC	NP_001291646.4:p.Tyr350Ala
NM_001304718.2:c.-63_-62delinsGC	NP_001291647.1:n.-63_-62delinsGC
NM_000314.8:c.529_530delinsGC MANE Select	NP_000305.3:p.Tyr177Ala