Canonical Allele Identifier: CA470974010

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89720782_89720783insA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961025_87961026insA , CM000672.2:g.87961025_87961026insA	GRCh38
NC_000010.10:g.89720782_89720783insA , CM000672.1:g.89720782_89720783insA	GRCh37
NC_000010.9:g.89710762_89710763insA	NCBI36
NG_007466.2:g.102587_102588insA , LRG_311:g.102587_102588insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1026_1027insA	ENSP00000514759.2:p.Asp343ArgfsTer13
ENST00000710265.1:c.933_934insA	ENSP00000518161.1:p.Asp312ArgfsTer13
ENST00000472832.3:c.933_934insA	ENSP00000483066.2:p.Asp312ArgfsTer13
ENST00000688158.2:n.1668_1669insA
ENST00000688922.2:c.*763_*764insA	ENSP00000508742.2:n.*763_*764insA
ENST00000700021.1:c.888_889insA	ENSP00000514757.1:p.Asp297ArgfsTer13
ENST00000700022.1:c.*272_*273insA	ENSP00000514758.1:n.*272_*273insA
ENST00000700023.1:n.2091_2092insA
ENST00000700024.1:n.2325_2326insA
ENST00000700025.1:n.1702_1703insA
ENST00000700026.1:n.570_571insA
ENST00000706954.1:c.933_934insA	ENSP00000516674.1:p.Asp312ArgfsTer13
ENST00000706955.1:c.*968_*969insA	ENSP00000516675.1:n.*968_*969insA
ENST00000686459.1:c.*519_*520insA	ENSP00000508909.1:n.*519_*520insA
ENST00000688158.1:c.*1044_*1045insA	ENSP00000509254.1:n.*1044_*1045insA
ENST00000688308.1:c.933_934insA	ENSP00000508752.1:p.Asp312ArgfsTer13
ENST00000688922.1:c.854_855insA
ENST00000693560.1:c.1452_1453insA	ENSP00000509861.1:p.Asp485ArgfsTer13
ENST00000371953.8:c.933_934insA MANE Select	ENSP00000361021.3:p.Asp312ArgfsTer13
ENST00000371953.7:c.933_934insA	ENSP00000361021.3:p.Asp312ArgfsTer13
ENST00000472832.2:c.360_361insA	ENSP00000483066.1:p.Asp121ArgfsTer13
NM_000314.5:c.933_934insA	NP_000305.3:p.Asp312ArgfsTer13
NM_000314.6:c.933_934insA	NP_000305.3:p.Asp312ArgfsTer13
NM_001304717.2:c.1452_1453insA	NP_001291646.2:p.Asp485ArgfsTer13
NM_001304718.1:c.342_343insA	NP_001291647.1:p.Asp115ArgfsTer13
XM_006717926.2:c.888_889insA	XP_006717989.1:p.Asp297ArgfsTer13
XM_011539981.1:c.933_934insA	XP_011538283.1:p.Asp312ArgfsTer13
XM_011539982.1:c.837_838insA	XP_011538284.1:p.Asp280ArgfsTer13
XR_945791.1:n.1503_1504insA
NM_000314.7:c.933_934insA	NP_000305.3:p.Asp312ArgfsTer13
NM_001304717.5:c.1452_1453insA	NP_001291646.4:p.Asp485ArgfsTer13
NM_001304718.2:c.342_343insA	NP_001291647.1:p.Asp115ArgfsTer13
NM_000314.8:c.933_934insA MANE Select	NP_000305.3:p.Asp312ArgfsTer13