Canonical Allele Identifier: CA891841100

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960952_87960953delinsGG , CM000672.2:g.87960952_87960953delinsGG	GRCh38
NC_000010.10:g.89720709_89720710delinsGG , CM000672.1:g.89720709_89720710delinsGG	GRCh37
NC_000010.9:g.89710689_89710690delinsGG	NCBI36
NG_007466.2:g.102514_102515delinsGG , LRG_311:g.102514_102515delinsGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.953_954delinsGG	ENSP00000514759.2:p.Ser318Trp
ENST00000710265.1:c.860_861delinsGG	ENSP00000518161.1:p.Ser287Trp
ENST00000472832.3:c.860_861delinsGG	ENSP00000483066.2:p.Ser287Trp
ENST00000688158.2:n.1595_1596delinsGG
ENST00000688922.2:c.*690_*691delinsGG	ENSP00000508742.2:n.*690_*691delinsGG
ENST00000700021.1:c.815_816delinsGG	ENSP00000514757.1:p.Ser272Trp
ENST00000700022.1:c.*199_*200delinsGG	ENSP00000514758.1:n.*199_*200delinsGG
ENST00000700023.1:n.2018_2019delinsGG
ENST00000700024.1:n.2252_2253delinsGG
ENST00000700025.1:n.1629_1630delinsGG
ENST00000700026.1:n.497_498delinsGG
ENST00000700029.1:c.787_788delinsGG
ENST00000706954.1:c.860_861delinsGG	ENSP00000516674.1:p.Ser287Trp
ENST00000706955.1:c.*895_*896delinsGG	ENSP00000516675.1:n.*895_*896delinsGG
ENST00000686459.1:c.*446_*447delinsGG	ENSP00000508909.1:n.*446_*447delinsGG
ENST00000688158.1:c.*971_*972delinsGG	ENSP00000509254.1:n.*971_*972delinsGG
ENST00000688308.1:c.860_861delinsGG	ENSP00000508752.1:p.Ser287Trp
ENST00000688922.1:c.781_782delinsGG
ENST00000693560.1:c.1379_1380delinsGG	ENSP00000509861.1:p.Ser460Trp
ENST00000371953.8:c.860_861delinsGG MANE Select	ENSP00000361021.3:p.Ser287Trp
ENST00000371953.7:c.860_861delinsGG	ENSP00000361021.3:p.Ser287Trp
ENST00000472832.2:c.287_288delinsGG	ENSP00000483066.1:p.Ser96Trp
NM_000314.5:c.860_861delinsGG	NP_000305.3:p.Ser287Trp
NM_000314.6:c.860_861delinsGG	NP_000305.3:p.Ser287Trp
NM_001304717.2:c.1379_1380delinsGG	NP_001291646.2:p.Ser460Trp
NM_001304718.1:c.269_270delinsGG	NP_001291647.1:p.Ser90Trp
XM_006717926.2:c.815_816delinsGG	XP_006717989.1:p.Ser272Trp
XM_011539981.1:c.860_861delinsGG	XP_011538283.1:p.Ser287Trp
XM_011539982.1:c.764_765delinsGG	XP_011538284.1:p.Ser255Trp
XR_945791.1:n.1430_1431delinsGG
NM_000314.7:c.860_861delinsGG	NP_000305.3:p.Ser287Trp
NM_001304717.5:c.1379_1380delinsGG	NP_001291646.4:p.Ser460Trp
NM_001304718.2:c.269_270delinsGG	NP_001291647.1:p.Ser90Trp
NM_000314.8:c.860_861delinsGG MANE Select	NP_000305.3:p.Ser287Trp