Canonical Allele Identifier: CA1926143060

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863514C= , CM000672.2:g.87863514C= GRCh38
NC_000010.10:g.89623271C= , CM000672.1:g.89623271C= GRCh37
NC_000010.9:g.89613251C= NCBI36
NG_007466.2:g.5077C= , LRG_311:g.5077C=
NG_033079.1:g.4924G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+872C= (PTEN) ENSP00000516674.1:n.-17+872C=
ENST00000688308.1:c.-17+401C= (PTEN) ENSP00000508752.1:n.-17+401C=
ENST00000693560.1:c.-436C= (PTEN) ENSP00000509861.1:n.-436C=
ENST00000445946.5:c.-1027G= (KLLN) MANE Select ENSP00000392204.2:n.-1027G=
ENST00000371953.7:c.-956C= (PTEN) ENSP00000361021.3:n.-956C=
ENST00000610634.1:c.-1058C= (PTEN) ENSP00000477517.1:n.-1058C=
NM_000314.5:c.-955C= (PTEN) NP_000305.3:n.-955C=
NM_000314.6:c.-955C= (PTEN) NP_000305.3:n.-955C=
NM_001304717.2:c.-436C= (PTEN) NP_001291646.2:n.-436C=
NM_001304718.1:c.-1660C= (PTEN) NP_001291647.1:n.-1660C=
NM_001126049.2:c.-1027G= (KLLN) MANE Select NP_001119521.1:n.-1027G=