Canonical Allele Identifier: CA891838755

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952146_87952147delinsGG , CM000672.2:g.87952146_87952147delinsGG	GRCh38
NC_000010.10:g.89711903_89711904delinsGG , CM000672.1:g.89711903_89711904delinsGG	GRCh37
NC_000010.9:g.89701883_89701884delinsGG	NCBI36
NG_007466.2:g.93708_93709delinsGG , LRG_311:g.93708_93709delinsGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.521_522delinsGG	ENSP00000514759.2:p.Tyr174Trp
ENST00000710265.1:c.521_522delinsGG	ENSP00000518161.1:p.Tyr174Trp
ENST00000472832.3:c.521_522delinsGG	ENSP00000483066.2:p.Tyr174Trp
ENST00000688158.2:n.1256_1257delinsGG
ENST00000688922.2:c.*351_*352delinsGG	ENSP00000508742.2:n.*351_*352delinsGG
ENST00000700021.1:c.476_477delinsGG	ENSP00000514757.1:p.Tyr159Trp
ENST00000700022.1:c.493-5707_493-5706delinsGG	ENSP00000514758.1:n.493-5707_493-5706deli...
ENST00000700023.1:n.1679_1680delinsGG
ENST00000700024.1:n.1913_1914delinsGG
ENST00000700025.1:n.1290_1291delinsGG
ENST00000700029.1:c.355_356delinsGG
ENST00000706954.1:c.521_522delinsGG	ENSP00000516674.1:p.Tyr174Trp
ENST00000706955.1:c.*556_*557delinsGG	ENSP00000516675.1:n.*556_*557delinsGG
ENST00000686459.1:c.*107_*108delinsGG	ENSP00000508909.1:n.*107_*108delinsGG
ENST00000688158.1:c.*632_*633delinsGG	ENSP00000509254.1:n.*632_*633delinsGG
ENST00000688308.1:c.521_522delinsGG	ENSP00000508752.1:p.Tyr174Trp
ENST00000688922.1:c.442_443delinsGG
ENST00000693560.1:c.1040_1041delinsGG	ENSP00000509861.1:p.Tyr347Trp
ENST00000371953.8:c.521_522delinsGG MANE Select	ENSP00000361021.3:p.Tyr174Trp
ENST00000371953.7:c.521_522delinsGG	ENSP00000361021.3:p.Tyr174Trp
NM_000314.5:c.521_522delinsGG	NP_000305.3:p.Tyr174Trp
NM_000314.6:c.521_522delinsGG	NP_000305.3:p.Tyr174Trp
NM_001304717.2:c.1040_1041delinsGG	NP_001291646.2:p.Tyr347Trp
NM_001304718.1:c.-71_-70delinsGG	NP_001291647.1:n.-71_-70delinsGG
XM_006717926.2:c.476_477delinsGG	XP_006717989.1:p.Tyr159Trp
XM_011539981.1:c.521_522delinsGG	XP_011538283.1:p.Tyr174Trp
XM_011539982.1:c.425_426delinsGG	XP_011538284.1:p.Tyr142Trp
XR_945789.1:n.1392_1393delinsGG
XR_945790.1:n.1509_1510delinsGG
XR_945791.1:n.1205-5707_1205-5706delinsGG
NM_000314.7:c.521_522delinsGG	NP_000305.3:p.Tyr174Trp
NM_001304717.5:c.1040_1041delinsGG	NP_001291646.4:p.Tyr347Trp
NM_001304718.2:c.-71_-70delinsGG	NP_001291647.1:n.-71_-70delinsGG
NM_000314.8:c.521_522delinsGG MANE Select	NP_000305.3:p.Tyr174Trp