Canonical Allele Identifier: CA2610046441
Gene: PTEN HGNC NCBI

Linked Data

gnomAD v4: 10-87863671-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863671G>T , CM000672.2:g.87863671G>T GRCh38
NC_000010.10:g.89623428G>T , CM000672.1:g.89623428G>T GRCh37
NC_000010.9:g.89613408G>T NCBI36
NG_007466.2:g.5234G>T , LRG_311:g.5234G>T
NG_033079.1:g.4767C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.-799G>T ENSP00000514759.2:n.-799G>T
ENST00000710265.1:c.-799G>T ENSP00000518161.1:n.-799G>T
ENST00000706954.1:c.-16-783G>T ENSP00000516674.1:n.-16-783G>T
ENST00000706955.1:c.-799G>T ENSP00000516675.1:n.-799G>T
ENST00000688158.1:c.-799G>T ENSP00000509254.1:n.-799G>T
ENST00000688308.1:c.-17+558G>T ENSP00000508752.1:n.-17+558G>T
ENST00000693560.1:c.-279G>T ENSP00000509861.1:n.-279G>T
ENST00000371953.8:c.-799G>T MANE Select ENSP00000361021.3:n.-799G>T
ENST00000371953.7:c.-799G>T ENSP00000361021.3:n.-799G>T
ENST00000610634.1:c.-901G>T ENSP00000477517.1:n.-901G>T
NM_000314.5:c.-798G>T NP_000305.3:n.-798G>T
NM_000314.6:c.-798G>T NP_000305.3:n.-798G>T
NM_001304717.2:c.-279G>T NP_001291646.2:n.-279G>T
NM_001304718.1:c.-1503G>T NP_001291647.1:n.-1503G>T
NM_000314.7:c.-798G>T NP_000305.3:n.-798G>T
NM_001304717.5:c.-279G>T NP_001291646.4:n.-279G>T
NM_001304718.2:c.-1503G>T NP_001291647.1:n.-1503G>T
NM_000314.8:c.-799G>T MANE Select NP_000305.3:n.-799G>T
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