Canonical Allele Identifier: CA891837359

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965341_87965343delinsTGG , CM000672.2:g.87965341_87965343delinsTGG	GRCh38
NC_000010.10:g.89725098_89725100delinsTGG , CM000672.1:g.89725098_89725100delinsTGG	GRCh37
NC_000010.9:g.89715078_89715080delinsTGG	NCBI36
NG_007466.2:g.106903_106905delinsTGG , LRG_311:g.106903_106905delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1174_1176delinsTGG	ENSP00000514759.2:p.Ser392Trp
ENST00000710265.1:c.*110_*112delinsTGG	ENSP00000518161.1:n.*110_*112delinsTGG
ENST00000688158.2:n.1816_1818delinsTGG
ENST00000688922.2:c.*911_*913delinsTGG	ENSP00000508742.2:n.*911_*913delinsTGG
ENST00000700021.1:c.1036_1038delinsTGG	ENSP00000514757.1:p.Ser346Trp
ENST00000700022.1:c.*420_*422delinsTGG	ENSP00000514758.1:n.*420_*422delinsTGG
ENST00000700023.1:n.2239_2241delinsTGG
ENST00000700024.1:n.2473_2475delinsTGG
ENST00000706954.1:c.1081_1083delinsTGG	ENSP00000516674.1:p.Ser361Trp
ENST00000706955.1:c.*1116_*1118delinsTGG	ENSP00000516675.1:n.*1116_*1118delinsTGG
ENST00000686459.1:c.*667_*669delinsTGG	ENSP00000508909.1:n.*667_*669delinsTGG
ENST00000688158.1:c.*1192_*1194delinsTGG	ENSP00000509254.1:n.*1192_*1194delinsTGG
ENST00000688308.1:c.1081_1083delinsTGG	ENSP00000508752.1:p.Ser361Trp
ENST00000688922.1:c.1002_1004delinsTGG
ENST00000693560.1:c.1600_1602delinsTGG	ENSP00000509861.1:p.Ser534Trp
ENST00000371953.8:c.1081_1083delinsTGG MANE Select	ENSP00000361021.3:p.Ser361Trp
ENST00000371953.7:c.1081_1083delinsTGG	ENSP00000361021.3:p.Ser361Trp
NM_000314.5:c.1081_1083delinsTGG	NP_000305.3:p.Ser361Trp
NM_000314.6:c.1081_1083delinsTGG	NP_000305.3:p.Ser361Trp
NM_001304717.2:c.1600_1602delinsTGG	NP_001291646.2:p.Ser534Trp
NM_001304718.1:c.490_492delinsTGG	NP_001291647.1:p.Ser164Trp
XM_006717926.2:c.1036_1038delinsTGG	XP_006717989.1:p.Ser346Trp
XM_011539982.1:c.985_987delinsTGG	XP_011538284.1:p.Ser329Trp
XR_945791.1:n.1651_1653delinsTGG
NM_000314.7:c.1081_1083delinsTGG	NP_000305.3:p.Ser361Trp
NM_001304717.5:c.1600_1602delinsTGG	NP_001291646.4:p.Ser534Trp
NM_001304718.2:c.490_492delinsTGG	NP_001291647.1:p.Ser164Trp
NM_000314.8:c.1081_1083delinsTGG MANE Select	NP_000305.3:p.Ser361Trp