Canonical Allele Identifier: CA377487411

Gene: PTEN

Linked Data

• dbSNP Id: rs786203911
• MyVariant Identifiers: chr10:g.89725188C>A (hg19) ; chr10:g.87965431C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965431C>A , CM000672.2:g.87965431C>A	GRCh38
NC_000010.10:g.89725188C>A , CM000672.1:g.89725188C>A	GRCh37
NC_000010.9:g.89715168C>A	NCBI36
NG_007466.2:g.106993C>A , LRG_311:g.106993C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1264C>A	ENSP00000514759.2:p.Pro422Thr
ENST00000710265.1:c.*200C>A	ENSP00000518161.1:n.*200C>A
ENST00000688158.2:n.1906C>A
ENST00000688922.2:c.*1001C>A	ENSP00000508742.2:n.*1001C>A
ENST00000700021.1:c.1126C>A	ENSP00000514757.1:p.Pro376Thr
ENST00000700022.1:c.*510C>A	ENSP00000514758.1:n.*510C>A
ENST00000700023.1:n.2329C>A
ENST00000700024.1:n.2563C>A
ENST00000706954.1:c.1171C>A	ENSP00000516674.1:p.Pro391Thr
ENST00000706955.1:c.*1206C>A	ENSP00000516675.1:n.*1206C>A
ENST00000686459.1:c.*757C>A	ENSP00000508909.1:n.*757C>A
ENST00000688158.1:c.*1282C>A	ENSP00000509254.1:n.*1282C>A
ENST00000688308.1:c.1171C>A	ENSP00000508752.1:p.Pro391Thr
ENST00000688922.1:c.1092C>A
ENST00000693560.1:c.1690C>A	ENSP00000509861.1:p.Pro564Thr
ENST00000371953.8:c.1171C>A MANE Select	ENSP00000361021.3:p.Pro391Thr
ENST00000371953.7:c.1171C>A	ENSP00000361021.3:p.Pro391Thr
NM_000314.5:c.1171C>A	NP_000305.3:p.Pro391Thr
NM_000314.6:c.1171C>A	NP_000305.3:p.Pro391Thr
NM_001304717.2:c.1690C>A	NP_001291646.2:p.Pro564Thr
NM_001304718.1:c.580C>A	NP_001291647.1:p.Pro194Thr
XM_006717926.2:c.1126C>A	XP_006717989.1:p.Pro376Thr
XM_011539982.1:c.1075C>A	XP_011538284.1:p.Pro359Thr
XR_945791.1:n.1741C>A
NM_000314.7:c.1171C>A	NP_000305.3:p.Pro391Thr
NM_001304717.5:c.1690C>A	NP_001291646.4:p.Pro564Thr
NM_001304718.2:c.580C>A	NP_001291647.1:p.Pro194Thr
NM_000314.8:c.1171C>A MANE Select	NP_000305.3:p.Pro391Thr