Canonical Allele Identifier: CA891839305

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957853_87957854delinsTG , CM000672.2:g.87957853_87957854delinsTG	GRCh38
NC_000010.10:g.89717610_89717611delinsTG , CM000672.1:g.89717610_89717611delinsTG	GRCh37
NC_000010.9:g.89707590_89707591delinsTG	NCBI36
NG_007466.2:g.99415_99416delinsTG , LRG_311:g.99415_99416delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.635_636delinsTG	ENSP00000514759.2:p.Asn212Met
ENST00000710265.1:c.635_636delinsTG	ENSP00000518161.1:p.Asn212Met
ENST00000472832.3:c.635_636delinsTG	ENSP00000483066.2:p.Asn212Met
ENST00000688158.2:n.1370_1371delinsTG
ENST00000688922.2:c.*465_*466delinsTG	ENSP00000508742.2:n.*465_*466delinsTG
ENST00000700021.1:c.590_591delinsTG	ENSP00000514757.1:p.Asn197Met
ENST00000700022.1:c.493_494delinsTG	ENSP00000514758.1:p.Ile165Cys
ENST00000700023.1:n.1793_1794delinsTG
ENST00000700024.1:n.2027_2028delinsTG
ENST00000700025.1:n.1404_1405delinsTG
ENST00000700026.1:n.272_273delinsTG
ENST00000700029.1:c.469_470delinsTG
ENST00000706954.1:c.635_636delinsTG	ENSP00000516674.1:p.Asn212Met
ENST00000706955.1:c.*670_*671delinsTG	ENSP00000516675.1:n.*670_*671delinsTG
ENST00000686459.1:c.*221_*222delinsTG	ENSP00000508909.1:n.*221_*222delinsTG
ENST00000688158.1:c.*746_*747delinsTG	ENSP00000509254.1:n.*746_*747delinsTG
ENST00000688308.1:c.635_636delinsTG	ENSP00000508752.1:p.Asn212Met
ENST00000688922.1:c.556_557delinsTG
ENST00000693560.1:c.1154_1155delinsTG	ENSP00000509861.1:p.Asn385Met
ENST00000371953.8:c.635_636delinsTG MANE Select	ENSP00000361021.3:p.Asn212Met
ENST00000371953.7:c.635_636delinsTG	ENSP00000361021.3:p.Asn212Met
ENST00000472832.2:c.62_63delinsTG	ENSP00000483066.1:p.Asn21Met
NM_000314.5:c.635_636delinsTG	NP_000305.3:p.Asn212Met
NM_000314.6:c.635_636delinsTG	NP_000305.3:p.Asn212Met
NM_001304717.2:c.1154_1155delinsTG	NP_001291646.2:p.Asn385Met
NM_001304718.1:c.44_45delinsTG	NP_001291647.1:p.Asn15Met
XM_006717926.2:c.590_591delinsTG	XP_006717989.1:p.Asn197Met
XM_011539981.1:c.635_636delinsTG	XP_011538283.1:p.Asn212Met
XM_011539982.1:c.539_540delinsTG	XP_011538284.1:p.Asn180Met
XR_945791.1:n.1205_1206delinsTG
NM_000314.7:c.635_636delinsTG	NP_000305.3:p.Asn212Met
NM_001304717.5:c.1154_1155delinsTG	NP_001291646.4:p.Asn385Met
NM_001304718.2:c.44_45delinsTG	NP_001291647.1:p.Asn15Met
NM_000314.8:c.635_636delinsTG MANE Select	NP_000305.3:p.Asn212Met