Canonical Allele Identifier: CA470974104

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89720840_89720841insA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961084dup , CM000672.2:g.87961084dup	GRCh38
NC_000010.10:g.89720841dup , CM000672.1:g.89720841dup	GRCh37
NC_000010.9:g.89710821dup	NCBI36
NG_007466.2:g.102646dup , LRG_311:g.102646dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1085dup	ENSP00000514759.2:p.Asp362GlufsTer12
ENST00000710265.1:c.992dup	ENSP00000518161.1:p.Asp331GlufsTer12
ENST00000472832.3:c.992dup	ENSP00000483066.2:p.Asp331GlufsTer12
ENST00000688158.2:n.1727dup
ENST00000688922.2:c.*822dup	ENSP00000508742.2:n.*822dup
ENST00000700021.1:c.947dup	ENSP00000514757.1:p.Asp316GlufsTer12
ENST00000700022.1:c.*331dup	ENSP00000514758.1:n.*331dup
ENST00000700023.1:n.2150dup
ENST00000700024.1:n.2384dup
ENST00000700025.1:n.1761dup
ENST00000700026.1:n.629dup
ENST00000706954.1:c.992dup	ENSP00000516674.1:p.Asp331GlufsTer12
ENST00000706955.1:c.*1027dup	ENSP00000516675.1:n.*1027dup
ENST00000686459.1:c.*578dup	ENSP00000508909.1:n.*578dup
ENST00000688158.1:c.*1103dup	ENSP00000509254.1:n.*1103dup
ENST00000688308.1:c.992dup	ENSP00000508752.1:p.Asp331GlufsTer12
ENST00000688922.1:c.913dup
ENST00000693560.1:c.1511dup	ENSP00000509861.1:p.Asp504GlufsTer12
ENST00000371953.8:c.992dup MANE Select	ENSP00000361021.3:p.Asp331GlufsTer12
ENST00000371953.7:c.992dup	ENSP00000361021.3:p.Asp331GlufsTer12
ENST00000472832.2:c.419dup	ENSP00000483066.1:p.Asp140GlufsTer12
NM_000314.5:c.992dup	NP_000305.3:p.Asp331GlufsTer12
NM_000314.6:c.992dup	NP_000305.3:p.Asp331GlufsTer12
NM_001304717.2:c.1511dup	NP_001291646.2:p.Asp504GlufsTer12
NM_001304718.1:c.401dup	NP_001291647.1:p.Asp134GlufsTer12
XM_006717926.2:c.947dup	XP_006717989.1:p.Asp316GlufsTer12
XM_011539981.1:c.992dup	XP_011538283.1:p.Asp331GlufsTer12
XM_011539982.1:c.896dup	XP_011538284.1:p.Asp299GlufsTer12
XR_945791.1:n.1562dup
NM_000314.7:c.992dup	NP_000305.3:p.Asp331GlufsTer12
NM_001304717.5:c.1511dup	NP_001291646.4:p.Asp504GlufsTer12
NM_001304718.2:c.401dup	NP_001291647.1:p.Asp134GlufsTer12
NM_000314.8:c.992dup MANE Select	NP_000305.3:p.Asp331GlufsTer12