Canonical Allele Identifier: CA470974029

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89720795_89720796insG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961038_87961039insG , CM000672.2:g.87961038_87961039insG	GRCh38
NC_000010.10:g.89720795_89720796insG , CM000672.1:g.89720795_89720796insG	GRCh37
NC_000010.9:g.89710775_89710776insG	NCBI36
NG_007466.2:g.102600_102601insG , LRG_311:g.102600_102601insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1039_1040insG	ENSP00000514759.2:p.Leu347ArgfsTer9
ENST00000710265.1:c.946_947insG	ENSP00000518161.1:p.Leu316ArgfsTer9
ENST00000472832.3:c.946_947insG	ENSP00000483066.2:p.Leu316ArgfsTer9
ENST00000688158.2:n.1681_1682insG
ENST00000688922.2:c.*776_*777insG	ENSP00000508742.2:n.*776_*777insG
ENST00000700021.1:c.901_902insG	ENSP00000514757.1:p.Leu301ArgfsTer9
ENST00000700022.1:c.*285_*286insG	ENSP00000514758.1:n.*285_*286insG
ENST00000700023.1:n.2104_2105insG
ENST00000700024.1:n.2338_2339insG
ENST00000700025.1:n.1715_1716insG
ENST00000700026.1:n.583_584insG
ENST00000706954.1:c.946_947insG	ENSP00000516674.1:p.Leu316ArgfsTer9
ENST00000706955.1:c.*981_*982insG	ENSP00000516675.1:n.*981_*982insG
ENST00000686459.1:c.*532_*533insG	ENSP00000508909.1:n.*532_*533insG
ENST00000688158.1:c.*1057_*1058insG	ENSP00000509254.1:n.*1057_*1058insG
ENST00000688308.1:c.946_947insG	ENSP00000508752.1:p.Leu316ArgfsTer9
ENST00000688922.1:c.867_868insG
ENST00000693560.1:c.1465_1466insG	ENSP00000509861.1:p.Leu489ArgfsTer9
ENST00000371953.8:c.946_947insG MANE Select	ENSP00000361021.3:p.Leu316ArgfsTer9
ENST00000371953.7:c.946_947insG	ENSP00000361021.3:p.Leu316ArgfsTer9
ENST00000472832.2:c.373_374insG	ENSP00000483066.1:p.Leu125ArgfsTer9
NM_000314.5:c.946_947insG	NP_000305.3:p.Leu316ArgfsTer9
NM_000314.6:c.946_947insG	NP_000305.3:p.Leu316ArgfsTer9
NM_001304717.2:c.1465_1466insG	NP_001291646.2:p.Leu489ArgfsTer9
NM_001304718.1:c.355_356insG	NP_001291647.1:p.Leu119ArgfsTer9
XM_006717926.2:c.901_902insG	XP_006717989.1:p.Leu301ArgfsTer9
XM_011539981.1:c.946_947insG	XP_011538283.1:p.Leu316ArgfsTer9
XM_011539982.1:c.850_851insG	XP_011538284.1:p.Leu284ArgfsTer9
XR_945791.1:n.1516_1517insG
NM_000314.7:c.946_947insG	NP_000305.3:p.Leu316ArgfsTer9
NM_001304717.5:c.1465_1466insG	NP_001291646.4:p.Leu489ArgfsTer9
NM_001304718.2:c.355_356insG	NP_001291647.1:p.Leu119ArgfsTer9
NM_000314.8:c.946_947insG MANE Select	NP_000305.3:p.Leu316ArgfsTer9