Canonical Allele Identifier: CA891838778

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952151_87952153delinsATG , CM000672.2:g.87952151_87952153delinsATG	GRCh38
NC_000010.10:g.89711908_89711910delinsATG , CM000672.1:g.89711908_89711910delinsATG	GRCh37
NC_000010.9:g.89701888_89701890delinsATG	NCBI36
NG_007466.2:g.93713_93715delinsATG , LRG_311:g.93713_93715delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.526_528delinsATG	ENSP00000514759.2:p.Tyr176Met
ENST00000710265.1:c.526_528delinsATG	ENSP00000518161.1:p.Tyr176Met
ENST00000472832.3:c.526_528delinsATG	ENSP00000483066.2:p.Tyr176Met
ENST00000688158.2:n.1261_1263delinsATG
ENST00000688922.2:c.*356_*358delinsATG	ENSP00000508742.2:n.*356_*358delinsATG
ENST00000700021.1:c.481_483delinsATG	ENSP00000514757.1:p.Tyr161Met
ENST00000700022.1:c.493-5702_493-5700delinsATG	ENSP00000514758.1:n.493-5702_493-5700delinsATG
ENST00000700023.1:n.1684_1686delinsATG
ENST00000700024.1:n.1918_1920delinsATG
ENST00000700025.1:n.1295_1297delinsATG
ENST00000700029.1:c.360_362delinsATG
ENST00000706954.1:c.526_528delinsATG	ENSP00000516674.1:p.Tyr176Met
ENST00000706955.1:c.*561_*563delinsATG	ENSP00000516675.1:n.*561_*563delinsATG
ENST00000686459.1:c.*112_*114delinsATG	ENSP00000508909.1:n.*112_*114delinsATG
ENST00000688158.1:c.*637_*639delinsATG	ENSP00000509254.1:n.*637_*639delinsATG
ENST00000688308.1:c.526_528delinsATG	ENSP00000508752.1:p.Tyr176Met
ENST00000688922.1:c.447_449delinsATG
ENST00000693560.1:c.1045_1047delinsATG	ENSP00000509861.1:p.Tyr349Met
ENST00000371953.8:c.526_528delinsATG MANE Select	ENSP00000361021.3:p.Tyr176Met
ENST00000371953.7:c.526_528delinsATG	ENSP00000361021.3:p.Tyr176Met
NM_000314.5:c.526_528delinsATG	NP_000305.3:p.Tyr176Met
NM_000314.6:c.526_528delinsATG	NP_000305.3:p.Tyr176Met
NM_001304717.2:c.1045_1047delinsATG	NP_001291646.2:p.Tyr349Met
NM_001304718.1:c.-66_-64delinsATG	NP_001291647.1:n.-66_-64delinsATG
XM_006717926.2:c.481_483delinsATG	XP_006717989.1:p.Tyr161Met
XM_011539981.1:c.526_528delinsATG	XP_011538283.1:p.Tyr176Met
XM_011539982.1:c.430_432delinsATG	XP_011538284.1:p.Tyr144Met
XR_945789.1:n.1397_1399delinsATG
XR_945790.1:n.1514_1516delinsATG
XR_945791.1:n.1205-5702_1205-5700delinsATG
NM_000314.7:c.526_528delinsATG	NP_000305.3:p.Tyr176Met
NM_001304717.5:c.1045_1047delinsATG	NP_001291646.4:p.Tyr349Met
NM_001304718.2:c.-66_-64delinsATG	NP_001291647.1:n.-66_-64delinsATG
NM_000314.8:c.526_528delinsATG MANE Select	NP_000305.3:p.Tyr176Met