Canonical Allele Identifier: CA377484811
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs2132276603

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957881G>T , CM000672.2:g.87957881G>T GRCh38
NC_000010.10:g.89717638G>T , CM000672.1:g.89717638G>T GRCh37
NC_000010.9:g.89707618G>T NCBI36
NG_007466.2:g.99443G>T , LRG_311:g.99443G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.663G>T ENSP00000514759.2:p.Lys221Asn
ENST00000710265.1:c.663G>T ENSP00000518161.1:p.Lys221Asn
ENST00000472832.3:c.663G>T ENSP00000483066.2:p.Lys221Asn
ENST00000688158.2:n.1398G>T
ENST00000688922.2:c.*493G>T ENSP00000508742.2:n.*493G>T
ENST00000700021.1:c.618G>T ENSP00000514757.1:p.Lys206Asn
ENST00000700022.1:c.*2G>T ENSP00000514758.1:n.*2G>T
ENST00000700023.1:n.1821G>T
ENST00000700024.1:n.2055G>T
ENST00000700025.1:n.1432G>T
ENST00000700026.1:n.300G>T
ENST00000700029.1:c.497G>T
ENST00000706954.1:c.663G>T ENSP00000516674.1:p.Lys221Asn
ENST00000706955.1:c.*698G>T ENSP00000516675.1:n.*698G>T
ENST00000686459.1:c.*249G>T ENSP00000508909.1:n.*249G>T
ENST00000688158.1:c.*774G>T ENSP00000509254.1:n.*774G>T
ENST00000688308.1:c.663G>T ENSP00000508752.1:p.Lys221Asn
ENST00000688922.1:c.584G>T
ENST00000693560.1:c.1182G>T ENSP00000509861.1:p.Lys394Asn
ENST00000371953.8:c.663G>T MANE Select ENSP00000361021.3:p.Lys221Asn
ENST00000371953.7:c.663G>T ENSP00000361021.3:p.Lys221Asn
ENST00000472832.2:c.90G>T ENSP00000483066.1:p.Lys30Asn
NM_000314.5:c.663G>T NP_000305.3:p.Lys221Asn
NM_000314.6:c.663G>T NP_000305.3:p.Lys221Asn
NM_001304717.2:c.1182G>T NP_001291646.2:p.Lys394Asn
NM_001304718.1:c.72G>T NP_001291647.1:p.Lys24Asn
XM_006717926.2:c.618G>T XP_006717989.1:p.Lys206Asn
XM_011539981.1:c.663G>T XP_011538283.1:p.Lys221Asn
XM_011539982.1:c.567G>T XP_011538284.1:p.Lys189Asn
XR_945791.1:n.1233G>T
NM_000314.7:c.663G>T NP_000305.3:p.Lys221Asn
NM_001304717.5:c.1182G>T NP_001291646.4:p.Lys394Asn
NM_001304718.2:c.72G>T NP_001291647.1:p.Lys24Asn
NM_000314.8:c.663G>T MANE Select NP_000305.3:p.Lys221Asn