Canonical Allele Identifier: CA891835266

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925551_87925552delinsGT , CM000672.2:g.87925551_87925552delinsGT	GRCh38
NC_000010.10:g.89685308_89685309delinsGT , CM000672.1:g.89685308_89685309delinsGT	GRCh37
NC_000010.9:g.89675288_89675289delinsGT	NCBI36
NG_007466.2:g.67113_67114delinsGT , LRG_311:g.67113_67114delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.203_204delinsGT	ENSP00000514759.2:p.Tyr68Cys
ENST00000710265.1:c.203_204delinsGT	ENSP00000518161.1:p.Tyr68Cys
ENST00000472832.3:c.203_204delinsGT	ENSP00000483066.2:p.Tyr68Cys
ENST00000688158.2:n.938_939delinsGT
ENST00000688922.2:c.203_204delinsGT	ENSP00000508742.2:p.Tyr68Cys
ENST00000700021.1:c.165-5495_165-5494delinsGT	ENSP00000514757.1:n.165-5495_165-5494delinsGT
ENST00000700022.1:c.203_204delinsGT	ENSP00000514758.1:p.Tyr68Cys
ENST00000700029.1:c.37_38delinsGT
ENST00000706954.1:c.203_204delinsGT	ENSP00000516674.1:p.Tyr68Cys
ENST00000706955.1:c.*238_*239delinsGT	ENSP00000516675.1:n.*238_*239delinsGT
ENST00000686459.1:c.203_204delinsGT	ENSP00000508909.1:p.Tyr68Cys
ENST00000688158.1:c.*314_*315delinsGT	ENSP00000509254.1:n.*314_*315delinsGT
ENST00000688308.1:c.203_204delinsGT	ENSP00000508752.1:p.Tyr68Cys
ENST00000688922.1:c.72_73delinsGT
ENST00000693560.1:c.722_723delinsGT	ENSP00000509861.1:p.Tyr241Cys
ENST00000371953.8:c.203_204delinsGT MANE Select	ENSP00000361021.3:p.Tyr68Cys
ENST00000371953.7:c.203_204delinsGT	ENSP00000361021.3:p.Tyr68Cys
ENST00000498703.1:n.29_30delinsGT
ENST00000610634.1:c.101_102delinsGT	ENSP00000477517.1:p.Tyr34Cys
NM_000314.5:c.203_204delinsGT	NP_000305.3:p.Tyr68Cys
NM_000314.6:c.203_204delinsGT	NP_000305.3:p.Tyr68Cys
NM_001304717.2:c.722_723delinsGT	NP_001291646.2:p.Tyr241Cys
NM_001304718.1:c.-541-5495_-541-5494delinsGT	NP_001291647.1:n.-541-5495_-541-5494delinsGT
XM_006717926.2:c.165-5495_165-5494delinsGT	XP_006717989.1:n.165-5495_165-5494delinsGT
XM_011539981.1:c.203_204delinsGT	XP_011538283.1:p.Tyr68Cys
XM_011539982.1:c.107_108delinsGT	XP_011538284.1:p.Tyr36Cys
XR_945789.1:n.915_916delinsGT
XR_945790.1:n.915_916delinsGT
XR_945791.1:n.915_916delinsGT
NM_000314.7:c.203_204delinsGT	NP_000305.3:p.Tyr68Cys
NM_001304717.5:c.722_723delinsGT	NP_001291646.4:p.Tyr241Cys
NM_001304718.2:c.-541-5495_-541-5494delinsGT	NP_001291647.1:n.-541-5495_-541-5494delinsGT
NM_000314.8:c.203_204delinsGT MANE Select	NP_000305.3:p.Tyr68Cys