Canonical Allele Identifier: CA377487465

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89725210C>A (hg19) ; chr10:g.87965453C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965453C>A , CM000672.2:g.87965453C>A	GRCh38
NC_000010.10:g.89725210C>A , CM000672.1:g.89725210C>A	GRCh37
NC_000010.9:g.89715190C>A	NCBI36
NG_007466.2:g.107015C>A , LRG_311:g.107015C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1286C>A	ENSP00000514759.2:p.Thr429Lys
ENST00000710265.1:c.*222C>A	ENSP00000518161.1:n.*222C>A
ENST00000688158.2:n.1928C>A
ENST00000688922.2:c.*1023C>A	ENSP00000508742.2:n.*1023C>A
ENST00000700021.1:c.1148C>A	ENSP00000514757.1:p.Thr383Lys
ENST00000700022.1:c.*532C>A	ENSP00000514758.1:n.*532C>A
ENST00000700023.1:n.2351C>A
ENST00000700024.1:n.2585C>A
ENST00000706954.1:c.1193C>A	ENSP00000516674.1:p.Thr398Lys
ENST00000706955.1:c.*1228C>A	ENSP00000516675.1:n.*1228C>A
ENST00000686459.1:c.*779C>A	ENSP00000508909.1:n.*779C>A
ENST00000688158.1:c.*1304C>A	ENSP00000509254.1:n.*1304C>A
ENST00000688308.1:c.1193C>A	ENSP00000508752.1:p.Thr398Lys
ENST00000688922.1:c.1114C>A
ENST00000693560.1:c.1712C>A	ENSP00000509861.1:p.Thr571Lys
ENST00000371953.8:c.1193C>A MANE Select	ENSP00000361021.3:p.Thr398Lys
ENST00000371953.7:c.1193C>A	ENSP00000361021.3:p.Thr398Lys
NM_000314.5:c.1193C>A	NP_000305.3:p.Thr398Lys
NM_000314.6:c.1193C>A	NP_000305.3:p.Thr398Lys
NM_001304717.2:c.1712C>A	NP_001291646.2:p.Thr571Lys
NM_001304718.1:c.602C>A	NP_001291647.1:p.Thr201Lys
XM_006717926.2:c.1148C>A	XP_006717989.1:p.Thr383Lys
XM_011539982.1:c.1097C>A	XP_011538284.1:p.Thr366Lys
XR_945791.1:n.1763C>A
NM_000314.7:c.1193C>A	NP_000305.3:p.Thr398Lys
NM_001304717.5:c.1712C>A	NP_001291646.4:p.Thr571Lys
NM_001304718.2:c.602C>A	NP_001291647.1:p.Thr201Lys
NM_000314.8:c.1193C>A MANE Select	NP_000305.3:p.Thr398Lys