Canonical Allele Identifier: CA891836655

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961057_87961058delinsTG , CM000672.2:g.87961057_87961058delinsTG	GRCh38
NC_000010.10:g.89720814_89720815delinsTG , CM000672.1:g.89720814_89720815delinsTG	GRCh37
NC_000010.9:g.89710794_89710795delinsTG	NCBI36
NG_007466.2:g.102619_102620delinsTG , LRG_311:g.102619_102620delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1058_1059delinsTG	ENSP00000514759.2:p.Lys353Met
ENST00000710265.1:c.965_966delinsTG	ENSP00000518161.1:p.Lys322Met
ENST00000472832.3:c.965_966delinsTG	ENSP00000483066.2:p.Lys322Met
ENST00000688158.2:n.1700_1701delinsTG
ENST00000688922.2:c.*795_*796delinsTG	ENSP00000508742.2:n.*795_*796delinsTG
ENST00000700021.1:c.920_921delinsTG	ENSP00000514757.1:p.Lys307Met
ENST00000700022.1:c.*304_*305delinsTG	ENSP00000514758.1:n.*304_*305delinsTG
ENST00000700023.1:n.2123_2124delinsTG
ENST00000700024.1:n.2357_2358delinsTG
ENST00000700025.1:n.1734_1735delinsTG
ENST00000700026.1:n.602_603delinsTG
ENST00000706954.1:c.965_966delinsTG	ENSP00000516674.1:p.Lys322Met
ENST00000706955.1:c.*1000_*1001delinsTG	ENSP00000516675.1:n.*1000_*1001delinsTG
ENST00000686459.1:c.*551_*552delinsTG	ENSP00000508909.1:n.*551_*552delinsTG
ENST00000688158.1:c.*1076_*1077delinsTG	ENSP00000509254.1:n.*1076_*1077delinsTG
ENST00000688308.1:c.965_966delinsTG	ENSP00000508752.1:p.Lys322Met
ENST00000688922.1:c.886_887delinsTG
ENST00000693560.1:c.1484_1485delinsTG	ENSP00000509861.1:p.Lys495Met
ENST00000371953.8:c.965_966delinsTG MANE Select	ENSP00000361021.3:p.Lys322Met
ENST00000371953.7:c.965_966delinsTG	ENSP00000361021.3:p.Lys322Met
ENST00000472832.2:c.392_393delinsTG	ENSP00000483066.1:p.Lys131Met
NM_000314.5:c.965_966delinsTG	NP_000305.3:p.Lys322Met
NM_000314.6:c.965_966delinsTG	NP_000305.3:p.Lys322Met
NM_001304717.2:c.1484_1485delinsTG	NP_001291646.2:p.Lys495Met
NM_001304718.1:c.374_375delinsTG	NP_001291647.1:p.Lys125Met
XM_006717926.2:c.920_921delinsTG	XP_006717989.1:p.Lys307Met
XM_011539981.1:c.965_966delinsTG	XP_011538283.1:p.Lys322Met
XM_011539982.1:c.869_870delinsTG	XP_011538284.1:p.Lys290Met
XR_945791.1:n.1535_1536delinsTG
NM_000314.7:c.965_966delinsTG	NP_000305.3:p.Lys322Met
NM_001304717.5:c.1484_1485delinsTG	NP_001291646.4:p.Lys495Met
NM_001304718.2:c.374_375delinsTG	NP_001291647.1:p.Lys125Met
NM_000314.8:c.965_966delinsTG MANE Select	NP_000305.3:p.Lys322Met