Canonical Allele Identifier: CA891837536

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933135_87933136delinsTA , CM000672.2:g.87933135_87933136delinsTA	GRCh38
NC_000010.10:g.89692892_89692893delinsTA , CM000672.1:g.89692892_89692893delinsTA	GRCh37
NC_000010.9:g.89682872_89682873delinsTA	NCBI36
NG_007466.2:g.74697_74698delinsTA , LRG_311:g.74697_74698delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.376_377delinsTA	ENSP00000514759.2:p.Ala126Tyr
ENST00000710265.1:c.376_377delinsTA	ENSP00000518161.1:p.Ala126Tyr
ENST00000472832.3:c.376_377delinsTA	ENSP00000483066.2:p.Ala126Tyr
ENST00000688158.2:n.1111_1112delinsTA
ENST00000688922.2:c.*206_*207delinsTA	ENSP00000508742.2:n.*206_*207delinsTA
ENST00000700021.1:c.331_332delinsTA	ENSP00000514757.1:p.Ala111Tyr
ENST00000700022.1:c.376_377delinsTA	ENSP00000514758.1:p.Ala126Tyr
ENST00000700029.1:c.210_211delinsTA
ENST00000706954.1:c.376_377delinsTA	ENSP00000516674.1:p.Ala126Tyr
ENST00000706955.1:c.*411_*412delinsTA	ENSP00000516675.1:n.*411_*412delinsTA
ENST00000686459.1:c.376_377delinsTA	ENSP00000508909.1:p.Ala126Tyr
ENST00000688158.1:c.*487_*488delinsTA	ENSP00000509254.1:n.*487_*488delinsTA
ENST00000688308.1:c.376_377delinsTA	ENSP00000508752.1:p.Ala126Tyr
ENST00000688922.1:c.297_298delinsTA
ENST00000693560.1:c.895_896delinsTA	ENSP00000509861.1:p.Ala299Tyr
ENST00000371953.8:c.376_377delinsTA MANE Select	ENSP00000361021.3:p.Ala126Tyr
ENST00000371953.7:c.376_377delinsTA	ENSP00000361021.3:p.Ala126Tyr
ENST00000498703.1:n.202_203delinsTA
ENST00000610634.1:c.274_275delinsTA	ENSP00000477517.1:p.Ala92Tyr
NM_000314.5:c.376_377delinsTA	NP_000305.3:p.Ala126Tyr
NM_000314.6:c.376_377delinsTA	NP_000305.3:p.Ala126Tyr
NM_001304717.2:c.895_896delinsTA	NP_001291646.2:p.Ala299Tyr
NM_001304718.1:c.-375_-374delinsTA	NP_001291647.1:n.-375_-374delinsTA
XM_006717926.2:c.331_332delinsTA	XP_006717989.1:p.Ala111Tyr
XM_011539981.1:c.376_377delinsTA	XP_011538283.1:p.Ala126Tyr
XM_011539982.1:c.280_281delinsTA	XP_011538284.1:p.Ala94Tyr
XR_945789.1:n.1088_1089delinsTA
XR_945790.1:n.1088_1089delinsTA
XR_945791.1:n.1088_1089delinsTA
NM_000314.7:c.376_377delinsTA	NP_000305.3:p.Ala126Tyr
NM_001304717.5:c.895_896delinsTA	NP_001291646.4:p.Ala299Tyr
NM_001304718.2:c.-375_-374delinsTA	NP_001291647.1:n.-375_-374delinsTA
NM_000314.8:c.376_377delinsTA MANE Select	NP_000305.3:p.Ala126Tyr