Canonical Allele Identifier: CA377784467
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs1554893782
MyVariant Identifiers: chr10:g.89653807G>C (hg19) chr10:g.87894050G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87894050G>C , CM000672.2:g.87894050G>C GRCh38
NC_000010.10:g.89653807G>C , CM000672.1:g.89653807G>C GRCh37
NC_000010.9:g.89643787G>C NCBI36
NG_007466.2:g.35612G>C , LRG_311:g.35612G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.105G>C ENSP00000514759.2:p.Met35Ile
ENST00000710265.1:c.105G>C ENSP00000518161.1:p.Met35Ile
ENST00000472832.3:c.105G>C ENSP00000483066.2:p.Met35Ile
ENST00000688158.2:n.899+13612G>C
ENST00000688922.2:c.105G>C ENSP00000508742.2:p.Met35Ile
ENST00000700021.1:c.105G>C ENSP00000514757.1:p.Met35Ile
ENST00000700022.1:c.105G>C ENSP00000514758.1:p.Met35Ile
ENST00000706954.1:c.105G>C ENSP00000516674.1:p.Met35Ile
ENST00000706955.1:c.*140G>C ENSP00000516675.1:n.*140G>C
ENST00000686459.1:c.105G>C ENSP00000508909.1:p.Met35Ile
ENST00000688158.1:c.*275+13612G>C ENSP00000509254.1:n.*275+13612G>C
ENST00000688308.1:c.105G>C ENSP00000508752.1:p.Met35Ile
ENST00000693560.1:c.624G>C ENSP00000509861.1:p.Met208Ile
ENST00000371953.8:c.105G>C MANE Select ENSP00000361021.3:p.Met35Ile
ENST00000371953.7:c.105G>C ENSP00000361021.3:p.Met35Ile
ENST00000462694.1:n.107G>C
ENST00000610634.1:c.3G>C ENSP00000477517.1:p.Met1Ile
NM_000314.5:c.105G>C NP_000305.3:p.Met35Ile
NM_000314.6:c.105G>C NP_000305.3:p.Met35Ile
NM_001304717.2:c.624G>C NP_001291646.2:p.Met208Ile
NM_001304718.1:c.-601G>C NP_001291647.1:n.-601G>C
XM_006717926.2:c.105G>C XP_006717989.1:p.Met35Ile
XM_011539981.1:c.105G>C XP_011538283.1:p.Met35Ile
XM_011539982.1:c.68+13612G>C XP_011538284.1:n.68+13612G>C
XR_945789.1:n.817G>C
XR_945790.1:n.817G>C
XR_945791.1:n.817G>C
NM_000314.7:c.105G>C NP_000305.3:p.Met35Ile
NM_001304717.5:c.624G>C NP_001291646.4:p.Met208Ile
NM_001304718.2:c.-601G>C NP_001291647.1:n.-601G>C
NM_000314.8:c.105G>C MANE Select NP_000305.3:p.Met35Ile
Search 100 bp 5'
Search 100 bp 3'