Canonical Allele Identifier: CA891841582

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965344_87965345delinsGT , CM000672.2:g.87965344_87965345delinsGT	GRCh38
NC_000010.10:g.89725101_89725102delinsGT , CM000672.1:g.89725101_89725102delinsGT	GRCh37
NC_000010.9:g.89715081_89715082delinsGT	NCBI36
NG_007466.2:g.106906_106907delinsGT , LRG_311:g.106906_106907delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1177_1178delinsGT	ENSP00000514759.2:p.Ser393Val
ENST00000710265.1:c.*113_*114delinsGT	ENSP00000518161.1:n.*113_*114delinsGT
ENST00000688158.2:n.1819_1820delinsGT
ENST00000688922.2:c.*914_*915delinsGT	ENSP00000508742.2:n.*914_*915delinsGT
ENST00000700021.1:c.1039_1040delinsGT	ENSP00000514757.1:p.Ser347Val
ENST00000700022.1:c.*423_*424delinsGT	ENSP00000514758.1:n.*423_*424delinsGT
ENST00000700023.1:n.2242_2243delinsGT
ENST00000700024.1:n.2476_2477delinsGT
ENST00000706954.1:c.1084_1085delinsGT	ENSP00000516674.1:p.Ser362Val
ENST00000706955.1:c.*1119_*1120delinsGT	ENSP00000516675.1:n.*1119_*1120delinsGT
ENST00000686459.1:c.*670_*671delinsGT	ENSP00000508909.1:n.*670_*671delinsGT
ENST00000688158.1:c.*1195_*1196delinsGT	ENSP00000509254.1:n.*1195_*1196delinsGT
ENST00000688308.1:c.1084_1085delinsGT	ENSP00000508752.1:p.Ser362Val
ENST00000688922.1:c.1005_1006delinsGT
ENST00000693560.1:c.1603_1604delinsGT	ENSP00000509861.1:p.Ser535Val
ENST00000371953.8:c.1084_1085delinsGT MANE Select	ENSP00000361021.3:p.Ser362Val
ENST00000371953.7:c.1084_1085delinsGT	ENSP00000361021.3:p.Ser362Val
NM_000314.5:c.1084_1085delinsGT	NP_000305.3:p.Ser362Val
NM_000314.6:c.1084_1085delinsGT	NP_000305.3:p.Ser362Val
NM_001304717.2:c.1603_1604delinsGT	NP_001291646.2:p.Ser535Val
NM_001304718.1:c.493_494delinsGT	NP_001291647.1:p.Ser165Val
XM_006717926.2:c.1039_1040delinsGT	XP_006717989.1:p.Ser347Val
XM_011539982.1:c.988_989delinsGT	XP_011538284.1:p.Ser330Val
XR_945791.1:n.1654_1655delinsGT
NM_000314.7:c.1084_1085delinsGT	NP_000305.3:p.Ser362Val
NM_001304717.5:c.1603_1604delinsGT	NP_001291646.4:p.Ser535Val
NM_001304718.2:c.493_494delinsGT	NP_001291647.1:p.Ser165Val
NM_000314.8:c.1084_1085delinsGT MANE Select	NP_000305.3:p.Ser362Val