Canonical Allele Identifier: CA891838687

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952134_87952135delinsTG , CM000672.2:g.87952134_87952135delinsTG	GRCh38
NC_000010.10:g.89711891_89711892delinsTG , CM000672.1:g.89711891_89711892delinsTG	GRCh37
NC_000010.9:g.89701871_89701872delinsTG	NCBI36
NG_007466.2:g.93696_93697delinsTG , LRG_311:g.93696_93697delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.509_510delinsTG	ENSP00000514759.2:p.Ser170Met
ENST00000710265.1:c.509_510delinsTG	ENSP00000518161.1:p.Ser170Met
ENST00000472832.3:c.509_510delinsTG	ENSP00000483066.2:p.Ser170Met
ENST00000688158.2:n.1244_1245delinsTG
ENST00000688922.2:c.*339_*340delinsTG	ENSP00000508742.2:n.*339_*340delinsTG
ENST00000700021.1:c.464_465delinsTG	ENSP00000514757.1:p.Ser155Met
ENST00000700022.1:c.493-5719_493-5718delinsTG	ENSP00000514758.1:n.493-5719_493-5718delinsTG
ENST00000700023.1:n.1667_1668delinsTG
ENST00000700024.1:n.1901_1902delinsTG
ENST00000700025.1:n.1278_1279delinsTG
ENST00000700029.1:c.343_344delinsTG
ENST00000706954.1:c.509_510delinsTG	ENSP00000516674.1:p.Ser170Met
ENST00000706955.1:c.*544_*545delinsTG	ENSP00000516675.1:n.*544_*545delinsTG
ENST00000686459.1:c.*95_*96delinsTG	ENSP00000508909.1:n.*95_*96delinsTG
ENST00000688158.1:c.*620_*621delinsTG	ENSP00000509254.1:n.*620_*621delinsTG
ENST00000688308.1:c.509_510delinsTG	ENSP00000508752.1:p.Ser170Met
ENST00000688922.1:c.430_431delinsTG
ENST00000693560.1:c.1028_1029delinsTG	ENSP00000509861.1:p.Ser343Met
ENST00000371953.8:c.509_510delinsTG MANE Select	ENSP00000361021.3:p.Ser170Met
ENST00000371953.7:c.509_510delinsTG	ENSP00000361021.3:p.Ser170Met
NM_000314.5:c.509_510delinsTG	NP_000305.3:p.Ser170Met
NM_000314.6:c.509_510delinsTG	NP_000305.3:p.Ser170Met
NM_001304717.2:c.1028_1029delinsTG	NP_001291646.2:p.Ser343Met
NM_001304718.1:c.-83_-82delinsTG	NP_001291647.1:n.-83_-82delinsTG
XM_006717926.2:c.464_465delinsTG	XP_006717989.1:p.Ser155Met
XM_011539981.1:c.509_510delinsTG	XP_011538283.1:p.Ser170Met
XM_011539982.1:c.413_414delinsTG	XP_011538284.1:p.Ser138Met
XR_945789.1:n.1380_1381delinsTG
XR_945790.1:n.1497_1498delinsTG
XR_945791.1:n.1205-5719_1205-5718delinsTG
NM_000314.7:c.509_510delinsTG	NP_000305.3:p.Ser170Met
NM_001304717.5:c.1028_1029delinsTG	NP_001291646.4:p.Ser343Met
NM_001304718.2:c.-83_-82delinsTG	NP_001291647.1:n.-83_-82delinsTG
NM_000314.8:c.509_510delinsTG MANE Select	NP_000305.3:p.Ser170Met