Canonical Allele Identifier: CA377784552

Gene: PTEN

Linked Data

• ClinVar Variation Id: 2562404
• ClinVar RCV Id: RCV003310464
• dbSNP Id: rs1114167672
• COSMIC: COSM5307
• MyVariant Identifiers: chr10:g.89653840C>G (hg19) ; chr10:g.87894083C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894083C>G , CM000672.2:g.87894083C>G	GRCh38
NC_000010.10:g.89653840C>G , CM000672.1:g.89653840C>G	GRCh37
NC_000010.9:g.89643820C>G	NCBI36
NG_007466.2:g.35645C>G , LRG_311:g.35645C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.138C>G	ENSP00000514759.2:p.Tyr46Ter
ENST00000710265.1:c.138C>G	ENSP00000518161.1:p.Tyr46Ter
ENST00000472832.3:c.138C>G	ENSP00000483066.2:p.Tyr46Ter
ENST00000688158.2:n.899+13645C>G
ENST00000688922.2:c.138C>G	ENSP00000508742.2:p.Tyr46Ter
ENST00000700021.1:c.138C>G	ENSP00000514757.1:p.Tyr46Ter
ENST00000700022.1:c.138C>G	ENSP00000514758.1:p.Tyr46Ter
ENST00000706954.1:c.138C>G	ENSP00000516674.1:p.Tyr46Ter
ENST00000706955.1:c.*173C>G	ENSP00000516675.1:n.*173C>G
ENST00000686459.1:c.138C>G	ENSP00000508909.1:p.Tyr46Ter
ENST00000688158.1:c.*275+13645C>G	ENSP00000509254.1:n.*275+13645C>G
ENST00000688308.1:c.138C>G	ENSP00000508752.1:p.Tyr46Ter
ENST00000688922.1:c.7C>G
ENST00000693560.1:c.657C>G	ENSP00000509861.1:p.Tyr219Ter
ENST00000371953.8:c.138C>G MANE Select	ENSP00000361021.3:p.Tyr46Ter
ENST00000371953.7:c.138C>G	ENSP00000361021.3:p.Tyr46Ter
ENST00000462694.1:n.140C>G
ENST00000610634.1:c.36C>G	ENSP00000477517.1:p.Tyr12Ter
NM_000314.5:c.138C>G	NP_000305.3:p.Tyr46Ter
NM_000314.6:c.138C>G	NP_000305.3:p.Tyr46Ter
NM_001304717.2:c.657C>G	NP_001291646.2:p.Tyr219Ter
NM_001304718.1:c.-568C>G	NP_001291647.1:n.-568C>G
XM_006717926.2:c.138C>G	XP_006717989.1:p.Tyr46Ter
XM_011539981.1:c.138C>G	XP_011538283.1:p.Tyr46Ter
XM_011539982.1:c.68+13645C>G	XP_011538284.1:n.68+13645C>G
XR_945789.1:n.850C>G
XR_945790.1:n.850C>G
XR_945791.1:n.850C>G
NM_000314.7:c.138C>G	NP_000305.3:p.Tyr46Ter
NM_001304717.5:c.657C>G	NP_001291646.4:p.Tyr219Ter
NM_001304718.2:c.-568C>G	NP_001291647.1:n.-568C>G
NM_000314.8:c.138C>G MANE Select	NP_000305.3:p.Tyr46Ter