Canonical Allele Identifier: CA891838794

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952155_87952156delinsGG , CM000672.2:g.87952155_87952156delinsGG	GRCh38
NC_000010.10:g.89711912_89711913delinsGG , CM000672.1:g.89711912_89711913delinsGG	GRCh37
NC_000010.9:g.89701892_89701893delinsGG	NCBI36
NG_007466.2:g.93717_93718delinsGG , LRG_311:g.93717_93718delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.530_531delinsGG	ENSP00000514759.2:p.Tyr177Trp
ENST00000710265.1:c.530_531delinsGG	ENSP00000518161.1:p.Tyr177Trp
ENST00000472832.3:c.530_531delinsGG	ENSP00000483066.2:p.Tyr177Trp
ENST00000688158.2:n.1265_1266delinsGG
ENST00000688922.2:c.*360_*361delinsGG	ENSP00000508742.2:n.*360_*361delinsGG
ENST00000700021.1:c.485_486delinsGG	ENSP00000514757.1:p.Tyr162Trp
ENST00000700022.1:c.493-5698_493-5697delinsGG	ENSP00000514758.1:n.493-5698_493-5697delinsGG
ENST00000700023.1:n.1688_1689delinsGG
ENST00000700024.1:n.1922_1923delinsGG
ENST00000700025.1:n.1299_1300delinsGG
ENST00000700029.1:c.364_365delinsGG
ENST00000706954.1:c.530_531delinsGG	ENSP00000516674.1:p.Tyr177Trp
ENST00000706955.1:c.*565_*566delinsGG	ENSP00000516675.1:n.*565_*566delinsGG
ENST00000686459.1:c.*116_*117delinsGG	ENSP00000508909.1:n.*116_*117delinsGG
ENST00000688158.1:c.*641_*642delinsGG	ENSP00000509254.1:n.*641_*642delinsGG
ENST00000688308.1:c.530_531delinsGG	ENSP00000508752.1:p.Tyr177Trp
ENST00000688922.1:c.451_452delinsGG
ENST00000693560.1:c.1049_1050delinsGG	ENSP00000509861.1:p.Tyr350Trp
ENST00000371953.8:c.530_531delinsGG MANE Select	ENSP00000361021.3:p.Tyr177Trp
ENST00000371953.7:c.530_531delinsGG	ENSP00000361021.3:p.Tyr177Trp
NM_000314.5:c.530_531delinsGG	NP_000305.3:p.Tyr177Trp
NM_000314.6:c.530_531delinsGG	NP_000305.3:p.Tyr177Trp
NM_001304717.2:c.1049_1050delinsGG	NP_001291646.2:p.Tyr350Trp
NM_001304718.1:c.-62_-61delinsGG	NP_001291647.1:n.-62_-61delinsGG
XM_006717926.2:c.485_486delinsGG	XP_006717989.1:p.Tyr162Trp
XM_011539981.1:c.530_531delinsGG	XP_011538283.1:p.Tyr177Trp
XM_011539982.1:c.434_435delinsGG	XP_011538284.1:p.Tyr145Trp
XR_945789.1:n.1401_1402delinsGG
XR_945790.1:n.1518_1519delinsGG
XR_945791.1:n.1205-5698_1205-5697delinsGG
NM_000314.7:c.530_531delinsGG	NP_000305.3:p.Tyr177Trp
NM_001304717.5:c.1049_1050delinsGG	NP_001291646.4:p.Tyr350Trp
NM_001304718.2:c.-62_-61delinsGG	NP_001291647.1:n.-62_-61delinsGG
NM_000314.8:c.530_531delinsGG MANE Select	NP_000305.3:p.Tyr177Trp