Canonical Allele Identifier: CA891841043

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960924_87960925delinsGA , CM000672.2:g.87960924_87960925delinsGA	GRCh38
NC_000010.10:g.89720681_89720682delinsGA , CM000672.1:g.89720681_89720682delinsGA	GRCh37
NC_000010.9:g.89710661_89710662delinsGA	NCBI36
NG_007466.2:g.102486_102487delinsGA , LRG_311:g.102486_102487delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.925_926delinsGA	ENSP00000514759.2:p.Phe309Asp
ENST00000710265.1:c.832_833delinsGA	ENSP00000518161.1:p.Phe278Asp
ENST00000472832.3:c.832_833delinsGA	ENSP00000483066.2:p.Phe278Asp
ENST00000688158.2:n.1567_1568delinsGA
ENST00000688922.2:c.*662_*663delinsGA	ENSP00000508742.2:n.*662_*663delinsGA
ENST00000700021.1:c.787_788delinsGA	ENSP00000514757.1:p.Phe263Asp
ENST00000700022.1:c.*171_*172delinsGA	ENSP00000514758.1:n.*171_*172delinsGA
ENST00000700023.1:n.1990_1991delinsGA
ENST00000700024.1:n.2224_2225delinsGA
ENST00000700025.1:n.1601_1602delinsGA
ENST00000700026.1:n.469_470delinsGA
ENST00000700029.1:c.759_760delinsGA
ENST00000706954.1:c.832_833delinsGA	ENSP00000516674.1:p.Phe278Asp
ENST00000706955.1:c.*867_*868delinsGA	ENSP00000516675.1:n.*867_*868delinsGA
ENST00000686459.1:c.*418_*419delinsGA	ENSP00000508909.1:n.*418_*419delinsGA
ENST00000688158.1:c.*943_*944delinsGA	ENSP00000509254.1:n.*943_*944delinsGA
ENST00000688308.1:c.832_833delinsGA	ENSP00000508752.1:p.Phe278Asp
ENST00000688922.1:c.753_754delinsGA
ENST00000693560.1:c.1351_1352delinsGA	ENSP00000509861.1:p.Phe451Asp
ENST00000371953.8:c.832_833delinsGA MANE Select	ENSP00000361021.3:p.Phe278Asp
ENST00000371953.7:c.832_833delinsGA	ENSP00000361021.3:p.Phe278Asp
ENST00000472832.2:c.259_260delinsGA	ENSP00000483066.1:p.Phe87Asp
NM_000314.5:c.832_833delinsGA	NP_000305.3:p.Phe278Asp
NM_000314.6:c.832_833delinsGA	NP_000305.3:p.Phe278Asp
NM_001304717.2:c.1351_1352delinsGA	NP_001291646.2:p.Phe451Asp
NM_001304718.1:c.241_242delinsGA	NP_001291647.1:p.Phe81Asp
XM_006717926.2:c.787_788delinsGA	XP_006717989.1:p.Phe263Asp
XM_011539981.1:c.832_833delinsGA	XP_011538283.1:p.Phe278Asp
XM_011539982.1:c.736_737delinsGA	XP_011538284.1:p.Phe246Asp
XR_945791.1:n.1402_1403delinsGA
NM_000314.7:c.832_833delinsGA	NP_000305.3:p.Phe278Asp
NM_001304717.5:c.1351_1352delinsGA	NP_001291646.4:p.Phe451Asp
NM_001304718.2:c.241_242delinsGA	NP_001291647.1:p.Phe81Asp
NM_000314.8:c.832_833delinsGA MANE Select	NP_000305.3:p.Phe278Asp