Canonical Allele Identifier: CA891835428

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960978_87960980delinsATG , CM000672.2:g.87960978_87960980delinsATG	GRCh38
NC_000010.10:g.89720735_89720737delinsATG , CM000672.1:g.89720735_89720737delinsATG	GRCh37
NC_000010.9:g.89710715_89710717delinsATG	NCBI36
NG_007466.2:g.102540_102542delinsATG , LRG_311:g.102540_102542delinsATG

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.979_981delinsATG	ENSP00000514759.2:p.Cys327Met
ENST00000710265.1:c.886_888delinsATG	ENSP00000518161.1:p.Cys296Met
ENST00000472832.3:c.886_888delinsATG	ENSP00000483066.2:p.Cys296Met
ENST00000688158.2:n.1621_1623delinsATG
ENST00000688922.2:c.*716_*718delinsATG	ENSP00000508742.2:n.*716_*718delinsATG
ENST00000700021.1:c.841_843delinsATG	ENSP00000514757.1:p.Cys281Met
ENST00000700022.1:c.*225_*227delinsATG	ENSP00000514758.1:n.*225_*227delinsATG
ENST00000700023.1:n.2044_2046delinsATG
ENST00000700024.1:n.2278_2280delinsATG
ENST00000700025.1:n.1655_1657delinsATG
ENST00000700026.1:n.523_525delinsATG
ENST00000706954.1:c.886_888delinsATG	ENSP00000516674.1:p.Cys296Met
ENST00000706955.1:c.*921_*923delinsATG	ENSP00000516675.1:n.*921_*923delinsATG
ENST00000686459.1:c.*472_*474delinsATG	ENSP00000508909.1:n.*472_*474delinsATG
ENST00000688158.1:c.*997_*999delinsATG	ENSP00000509254.1:n.*997_*999delinsATG
ENST00000688308.1:c.886_888delinsATG	ENSP00000508752.1:p.Cys296Met
ENST00000688922.1:c.807_809delinsATG
ENST00000693560.1:c.1405_1407delinsATG	ENSP00000509861.1:p.Cys469Met
ENST00000371953.8:c.886_888delinsATG MANE Select	ENSP00000361021.3:p.Cys296Met
ENST00000371953.7:c.886_888delinsATG	ENSP00000361021.3:p.Cys296Met
ENST00000472832.2:c.313_315delinsATG	ENSP00000483066.1:p.Cys105Met
NM_000314.5:c.886_888delinsATG	NP_000305.3:p.Cys296Met
NM_000314.6:c.886_888delinsATG	NP_000305.3:p.Cys296Met
NM_001304717.2:c.1405_1407delinsATG	NP_001291646.2:p.Cys469Met
NM_001304718.1:c.295_297delinsATG	NP_001291647.1:p.Cys99Met
XM_006717926.2:c.841_843delinsATG	XP_006717989.1:p.Cys281Met
XM_011539981.1:c.886_888delinsATG	XP_011538283.1:p.Cys296Met
XM_011539982.1:c.790_792delinsATG	XP_011538284.1:p.Cys264Met
XR_945791.1:n.1456_1458delinsATG
NM_000314.7:c.886_888delinsATG	NP_000305.3:p.Cys296Met
NM_001304717.5:c.1405_1407delinsATG	NP_001291646.4:p.Cys469Met
NM_001304718.2:c.295_297delinsATG	NP_001291647.1:p.Cys99Met
NM_000314.8:c.886_888delinsATG MANE Select	NP_000305.3:p.Cys296Met