Canonical Allele Identifier: CA891838754

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952145_87952147delinsATG , CM000672.2:g.87952145_87952147delinsATG	GRCh38
NC_000010.10:g.89711902_89711904delinsATG , CM000672.1:g.89711902_89711904delinsATG	GRCh37
NC_000010.9:g.89701882_89701884delinsATG	NCBI36
NG_007466.2:g.93707_93709delinsATG , LRG_311:g.93707_93709delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.520_522delinsATG	ENSP00000514759.2:p.Tyr174Met
ENST00000710265.1:c.520_522delinsATG	ENSP00000518161.1:p.Tyr174Met
ENST00000472832.3:c.520_522delinsATG	ENSP00000483066.2:p.Tyr174Met
ENST00000688158.2:n.1255_1257delinsATG
ENST00000688922.2:c.*350_*352delinsATG	ENSP00000508742.2:n.*350_*352delinsATG
ENST00000700021.1:c.475_477delinsATG	ENSP00000514757.1:p.Tyr159Met
ENST00000700022.1:c.493-5708_493-5706delinsATG	ENSP00000514758.1:n.493-5708_493-5706delinsATG
ENST00000700023.1:n.1678_1680delinsATG
ENST00000700024.1:n.1912_1914delinsATG
ENST00000700025.1:n.1289_1291delinsATG
ENST00000700029.1:c.354_356delinsATG
ENST00000706954.1:c.520_522delinsATG	ENSP00000516674.1:p.Tyr174Met
ENST00000706955.1:c.*555_*557delinsATG	ENSP00000516675.1:n.*555_*557delinsATG
ENST00000686459.1:c.*106_*108delinsATG	ENSP00000508909.1:n.*106_*108delinsATG
ENST00000688158.1:c.*631_*633delinsATG	ENSP00000509254.1:n.*631_*633delinsATG
ENST00000688308.1:c.520_522delinsATG	ENSP00000508752.1:p.Tyr174Met
ENST00000688922.1:c.441_443delinsATG
ENST00000693560.1:c.1039_1041delinsATG	ENSP00000509861.1:p.Tyr347Met
ENST00000371953.8:c.520_522delinsATG MANE Select	ENSP00000361021.3:p.Tyr174Met
ENST00000371953.7:c.520_522delinsATG	ENSP00000361021.3:p.Tyr174Met
NM_000314.5:c.520_522delinsATG	NP_000305.3:p.Tyr174Met
NM_000314.6:c.520_522delinsATG	NP_000305.3:p.Tyr174Met
NM_001304717.2:c.1039_1041delinsATG	NP_001291646.2:p.Tyr347Met
NM_001304718.1:c.-72_-70delinsATG	NP_001291647.1:n.-72_-70delinsATG
XM_006717926.2:c.475_477delinsATG	XP_006717989.1:p.Tyr159Met
XM_011539981.1:c.520_522delinsATG	XP_011538283.1:p.Tyr174Met
XM_011539982.1:c.424_426delinsATG	XP_011538284.1:p.Tyr142Met
XR_945789.1:n.1391_1393delinsATG
XR_945790.1:n.1508_1510delinsATG
XR_945791.1:n.1205-5708_1205-5706delinsATG
NM_000314.7:c.520_522delinsATG	NP_000305.3:p.Tyr174Met
NM_001304717.5:c.1039_1041delinsATG	NP_001291646.4:p.Tyr347Met
NM_001304718.2:c.-72_-70delinsATG	NP_001291647.1:n.-72_-70delinsATG
NM_000314.8:c.520_522delinsATG MANE Select	NP_000305.3:p.Tyr174Met