Canonical Allele Identifier: CA891838781

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952152_87952153delinsGG , CM000672.2:g.87952152_87952153delinsGG	GRCh38
NC_000010.10:g.89711909_89711910delinsGG , CM000672.1:g.89711909_89711910delinsGG	GRCh37
NC_000010.9:g.89701889_89701890delinsGG	NCBI36
NG_007466.2:g.93714_93715delinsGG , LRG_311:g.93714_93715delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.527_528delinsGG	ENSP00000514759.2:p.Tyr176Trp
ENST00000710265.1:c.527_528delinsGG	ENSP00000518161.1:p.Tyr176Trp
ENST00000472832.3:c.527_528delinsGG	ENSP00000483066.2:p.Tyr176Trp
ENST00000688158.2:n.1262_1263delinsGG
ENST00000688922.2:c.*357_*358delinsGG	ENSP00000508742.2:n.*357_*358delinsGG
ENST00000700021.1:c.482_483delinsGG	ENSP00000514757.1:p.Tyr161Trp
ENST00000700022.1:c.493-5701_493-5700delinsGG	ENSP00000514758.1:n.493-5701_493-5700delinsGG
ENST00000700023.1:n.1685_1686delinsGG
ENST00000700024.1:n.1919_1920delinsGG
ENST00000700025.1:n.1296_1297delinsGG
ENST00000700029.1:c.361_362delinsGG
ENST00000706954.1:c.527_528delinsGG	ENSP00000516674.1:p.Tyr176Trp
ENST00000706955.1:c.*562_*563delinsGG	ENSP00000516675.1:n.*562_*563delinsGG
ENST00000686459.1:c.*113_*114delinsGG	ENSP00000508909.1:n.*113_*114delinsGG
ENST00000688158.1:c.*638_*639delinsGG	ENSP00000509254.1:n.*638_*639delinsGG
ENST00000688308.1:c.527_528delinsGG	ENSP00000508752.1:p.Tyr176Trp
ENST00000688922.1:c.448_449delinsGG
ENST00000693560.1:c.1046_1047delinsGG	ENSP00000509861.1:p.Tyr349Trp
ENST00000371953.8:c.527_528delinsGG MANE Select	ENSP00000361021.3:p.Tyr176Trp
ENST00000371953.7:c.527_528delinsGG	ENSP00000361021.3:p.Tyr176Trp
NM_000314.5:c.527_528delinsGG	NP_000305.3:p.Tyr176Trp
NM_000314.6:c.527_528delinsGG	NP_000305.3:p.Tyr176Trp
NM_001304717.2:c.1046_1047delinsGG	NP_001291646.2:p.Tyr349Trp
NM_001304718.1:c.-65_-64delinsGG	NP_001291647.1:n.-65_-64delinsGG
XM_006717926.2:c.482_483delinsGG	XP_006717989.1:p.Tyr161Trp
XM_011539981.1:c.527_528delinsGG	XP_011538283.1:p.Tyr176Trp
XM_011539982.1:c.431_432delinsGG	XP_011538284.1:p.Tyr144Trp
XR_945789.1:n.1398_1399delinsGG
XR_945790.1:n.1515_1516delinsGG
XR_945791.1:n.1205-5701_1205-5700delinsGG
NM_000314.7:c.527_528delinsGG	NP_000305.3:p.Tyr176Trp
NM_001304717.5:c.1046_1047delinsGG	NP_001291646.4:p.Tyr349Trp
NM_001304718.2:c.-65_-64delinsGG	NP_001291647.1:n.-65_-64delinsGG
NM_000314.8:c.527_528delinsGG MANE Select	NP_000305.3:p.Tyr176Trp