Canonical Allele Identifier: CA891835265

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925551_87925552delinsCT , CM000672.2:g.87925551_87925552delinsCT	GRCh38
NC_000010.10:g.89685308_89685309delinsCT , CM000672.1:g.89685308_89685309delinsCT	GRCh37
NC_000010.9:g.89675288_89675289delinsCT	NCBI36
NG_007466.2:g.67113_67114delinsCT , LRG_311:g.67113_67114delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.203_204delinsCT	ENSP00000514759.2:p.Tyr68Ser
ENST00000710265.1:c.203_204delinsCT	ENSP00000518161.1:p.Tyr68Ser
ENST00000472832.3:c.203_204delinsCT	ENSP00000483066.2:p.Tyr68Ser
ENST00000688158.2:n.938_939delinsCT
ENST00000688922.2:c.203_204delinsCT	ENSP00000508742.2:p.Tyr68Ser
ENST00000700021.1:c.165-5495_165-5494delinsCT	ENSP00000514757.1:n.165-5495_165-5494delinsCT
ENST00000700022.1:c.203_204delinsCT	ENSP00000514758.1:p.Tyr68Ser
ENST00000700029.1:c.37_38delinsCT
ENST00000706954.1:c.203_204delinsCT	ENSP00000516674.1:p.Tyr68Ser
ENST00000706955.1:c.*238_*239delinsCT	ENSP00000516675.1:n.*238_*239delinsCT
ENST00000686459.1:c.203_204delinsCT	ENSP00000508909.1:p.Tyr68Ser
ENST00000688158.1:c.*314_*315delinsCT	ENSP00000509254.1:n.*314_*315delinsCT
ENST00000688308.1:c.203_204delinsCT	ENSP00000508752.1:p.Tyr68Ser
ENST00000688922.1:c.72_73delinsCT
ENST00000693560.1:c.722_723delinsCT	ENSP00000509861.1:p.Tyr241Ser
ENST00000371953.8:c.203_204delinsCT MANE Select	ENSP00000361021.3:p.Tyr68Ser
ENST00000371953.7:c.203_204delinsCT	ENSP00000361021.3:p.Tyr68Ser
ENST00000498703.1:n.29_30delinsCT
ENST00000610634.1:c.101_102delinsCT	ENSP00000477517.1:p.Tyr34Ser
NM_000314.5:c.203_204delinsCT	NP_000305.3:p.Tyr68Ser
NM_000314.6:c.203_204delinsCT	NP_000305.3:p.Tyr68Ser
NM_001304717.2:c.722_723delinsCT	NP_001291646.2:p.Tyr241Ser
NM_001304718.1:c.-541-5495_-541-5494delinsCT	NP_001291647.1:n.-541-5495_-541-5494delinsCT
XM_006717926.2:c.165-5495_165-5494delinsCT	XP_006717989.1:n.165-5495_165-5494delinsCT
XM_011539981.1:c.203_204delinsCT	XP_011538283.1:p.Tyr68Ser
XM_011539982.1:c.107_108delinsCT	XP_011538284.1:p.Tyr36Ser
XR_945789.1:n.915_916delinsCT
XR_945790.1:n.915_916delinsCT
XR_945791.1:n.915_916delinsCT
NM_000314.7:c.203_204delinsCT	NP_000305.3:p.Tyr68Ser
NM_001304717.5:c.722_723delinsCT	NP_001291646.4:p.Tyr241Ser
NM_001304718.2:c.-541-5495_-541-5494delinsCT	NP_001291647.1:n.-541-5495_-541-5494delinsCT
NM_000314.8:c.203_204delinsCT MANE Select	NP_000305.3:p.Tyr68Ser