Canonical Allele Identifier: CA891841581

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965344_87965345delinsGG , CM000672.2:g.87965344_87965345delinsGG	GRCh38
NC_000010.10:g.89725101_89725102delinsGG , CM000672.1:g.89725101_89725102delinsGG	GRCh37
NC_000010.9:g.89715081_89715082delinsGG	NCBI36
NG_007466.2:g.106906_106907delinsGG , LRG_311:g.106906_106907delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1177_1178delinsGG	ENSP00000514759.2:p.Ser393Gly
ENST00000710265.1:c.*113_*114delinsGG	ENSP00000518161.1:n.*113_*114delinsGG
ENST00000688158.2:n.1819_1820delinsGG
ENST00000688922.2:c.*914_*915delinsGG	ENSP00000508742.2:n.*914_*915delinsGG
ENST00000700021.1:c.1039_1040delinsGG	ENSP00000514757.1:p.Ser347Gly
ENST00000700022.1:c.*423_*424delinsGG	ENSP00000514758.1:n.*423_*424delinsGG
ENST00000700023.1:n.2242_2243delinsGG
ENST00000700024.1:n.2476_2477delinsGG
ENST00000706954.1:c.1084_1085delinsGG	ENSP00000516674.1:p.Ser362Gly
ENST00000706955.1:c.*1119_*1120delinsGG	ENSP00000516675.1:n.*1119_*1120delinsGG
ENST00000686459.1:c.*670_*671delinsGG	ENSP00000508909.1:n.*670_*671delinsGG
ENST00000688158.1:c.*1195_*1196delinsGG	ENSP00000509254.1:n.*1195_*1196delinsGG
ENST00000688308.1:c.1084_1085delinsGG	ENSP00000508752.1:p.Ser362Gly
ENST00000688922.1:c.1005_1006delinsGG
ENST00000693560.1:c.1603_1604delinsGG	ENSP00000509861.1:p.Ser535Gly
ENST00000371953.8:c.1084_1085delinsGG MANE Select	ENSP00000361021.3:p.Ser362Gly
ENST00000371953.7:c.1084_1085delinsGG	ENSP00000361021.3:p.Ser362Gly
NM_000314.5:c.1084_1085delinsGG	NP_000305.3:p.Ser362Gly
NM_000314.6:c.1084_1085delinsGG	NP_000305.3:p.Ser362Gly
NM_001304717.2:c.1603_1604delinsGG	NP_001291646.2:p.Ser535Gly
NM_001304718.1:c.493_494delinsGG	NP_001291647.1:p.Ser165Gly
XM_006717926.2:c.1039_1040delinsGG	XP_006717989.1:p.Ser347Gly
XM_011539982.1:c.988_989delinsGG	XP_011538284.1:p.Ser330Gly
XR_945791.1:n.1654_1655delinsGG
NM_000314.7:c.1084_1085delinsGG	NP_000305.3:p.Ser362Gly
NM_001304717.5:c.1603_1604delinsGG	NP_001291646.4:p.Ser535Gly
NM_001304718.2:c.493_494delinsGG	NP_001291647.1:p.Ser165Gly
NM_000314.8:c.1084_1085delinsGG MANE Select	NP_000305.3:p.Ser362Gly