Canonical Allele Identifier: CA377487289

Gene: PTEN

Linked Data

• dbSNP Id: rs2132289835
• MyVariant Identifiers: chr10:g.89725137C>A (hg19) ; chr10:g.87965380C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965380C>A , CM000672.2:g.87965380C>A	GRCh38
NC_000010.10:g.89725137C>A , CM000672.1:g.89725137C>A	GRCh37
NC_000010.9:g.89715117C>A	NCBI36
NG_007466.2:g.106942C>A , LRG_311:g.106942C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1213C>A	ENSP00000514759.2:p.Pro405Thr
ENST00000710265.1:c.*149C>A	ENSP00000518161.1:n.*149C>A
ENST00000688158.2:n.1855C>A
ENST00000688922.2:c.*950C>A	ENSP00000508742.2:n.*950C>A
ENST00000700021.1:c.1075C>A	ENSP00000514757.1:p.Pro359Thr
ENST00000700022.1:c.*459C>A	ENSP00000514758.1:n.*459C>A
ENST00000700023.1:n.2278C>A
ENST00000700024.1:n.2512C>A
ENST00000706954.1:c.1120C>A	ENSP00000516674.1:p.Pro374Thr
ENST00000706955.1:c.*1155C>A	ENSP00000516675.1:n.*1155C>A
ENST00000686459.1:c.*706C>A	ENSP00000508909.1:n.*706C>A
ENST00000688158.1:c.*1231C>A	ENSP00000509254.1:n.*1231C>A
ENST00000688308.1:c.1120C>A	ENSP00000508752.1:p.Pro374Thr
ENST00000688922.1:c.1041C>A
ENST00000693560.1:c.1639C>A	ENSP00000509861.1:p.Pro547Thr
ENST00000371953.8:c.1120C>A MANE Select	ENSP00000361021.3:p.Pro374Thr
ENST00000371953.7:c.1120C>A	ENSP00000361021.3:p.Pro374Thr
NM_000314.5:c.1120C>A	NP_000305.3:p.Pro374Thr
NM_000314.6:c.1120C>A	NP_000305.3:p.Pro374Thr
NM_001304717.2:c.1639C>A	NP_001291646.2:p.Pro547Thr
NM_001304718.1:c.529C>A	NP_001291647.1:p.Pro177Thr
XM_006717926.2:c.1075C>A	XP_006717989.1:p.Pro359Thr
XM_011539982.1:c.1024C>A	XP_011538284.1:p.Pro342Thr
XR_945791.1:n.1690C>A
NM_000314.7:c.1120C>A	NP_000305.3:p.Pro374Thr
NM_001304717.5:c.1639C>A	NP_001291646.4:p.Pro547Thr
NM_001304718.2:c.529C>A	NP_001291647.1:p.Pro177Thr
NM_000314.8:c.1120C>A MANE Select	NP_000305.3:p.Pro374Thr