Canonical Allele Identifier: CA891836180

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961017_87961019delinsTAT , CM000672.2:g.87961017_87961019delinsTAT	GRCh38
NC_000010.10:g.89720774_89720776delinsTAT , CM000672.1:g.89720774_89720776delinsTAT	GRCh37
NC_000010.9:g.89710754_89710756delinsTAT	NCBI36
NG_007466.2:g.102579_102581delinsTAT , LRG_311:g.102579_102581delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1018_1020delinsTAT	ENSP00000514759.2:p.Ala340Tyr
ENST00000710265.1:c.925_927delinsTAT	ENSP00000518161.1:p.Ala309Tyr
ENST00000472832.3:c.925_927delinsTAT	ENSP00000483066.2:p.Ala309Tyr
ENST00000688158.2:n.1660_1662delinsTAT
ENST00000688922.2:c.*755_*757delinsTAT	ENSP00000508742.2:n.*755_*757delinsTAT
ENST00000700021.1:c.880_882delinsTAT	ENSP00000514757.1:p.Ala294Tyr
ENST00000700022.1:c.*264_*266delinsTAT	ENSP00000514758.1:n.*264_*266delinsTAT
ENST00000700023.1:n.2083_2085delinsTAT
ENST00000700024.1:n.2317_2319delinsTAT
ENST00000700025.1:n.1694_1696delinsTAT
ENST00000700026.1:n.562_564delinsTAT
ENST00000706954.1:c.925_927delinsTAT	ENSP00000516674.1:p.Ala309Tyr
ENST00000706955.1:c.*960_*962delinsTAT	ENSP00000516675.1:n.*960_*962delinsTAT
ENST00000686459.1:c.*511_*513delinsTAT	ENSP00000508909.1:n.*511_*513delinsTAT
ENST00000688158.1:c.*1036_*1038delinsTAT	ENSP00000509254.1:n.*1036_*1038delinsTAT
ENST00000688308.1:c.925_927delinsTAT	ENSP00000508752.1:p.Ala309Tyr
ENST00000688922.1:c.846_848delinsTAT
ENST00000693560.1:c.1444_1446delinsTAT	ENSP00000509861.1:p.Ala482Tyr
ENST00000371953.8:c.925_927delinsTAT MANE Select	ENSP00000361021.3:p.Ala309Tyr
ENST00000371953.7:c.925_927delinsTAT	ENSP00000361021.3:p.Ala309Tyr
ENST00000472832.2:c.352_354delinsTAT	ENSP00000483066.1:p.Ala118Tyr
NM_000314.5:c.925_927delinsTAT	NP_000305.3:p.Ala309Tyr
NM_000314.6:c.925_927delinsTAT	NP_000305.3:p.Ala309Tyr
NM_001304717.2:c.1444_1446delinsTAT	NP_001291646.2:p.Ala482Tyr
NM_001304718.1:c.334_336delinsTAT	NP_001291647.1:p.Ala112Tyr
XM_006717926.2:c.880_882delinsTAT	XP_006717989.1:p.Ala294Tyr
XM_011539981.1:c.925_927delinsTAT	XP_011538283.1:p.Ala309Tyr
XM_011539982.1:c.829_831delinsTAT	XP_011538284.1:p.Ala277Tyr
XR_945791.1:n.1495_1497delinsTAT
NM_000314.7:c.925_927delinsTAT	NP_000305.3:p.Ala309Tyr
NM_001304717.5:c.1444_1446delinsTAT	NP_001291646.4:p.Ala482Tyr
NM_001304718.2:c.334_336delinsTAT	NP_001291647.1:p.Ala112Tyr
NM_000314.8:c.925_927delinsTAT MANE Select	NP_000305.3:p.Ala309Tyr