Canonical Allele Identifier: CA1926143156

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863620G= , CM000672.2:g.87863620G= GRCh38
NC_000010.10:g.89623377G= , CM000672.1:g.89623377G= GRCh37
NC_000010.9:g.89613357G= NCBI36
NG_007466.2:g.5183G= , LRG_311:g.5183G=
NG_033079.1:g.4818C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-834G= (PTEN) ENSP00000516674.1:n.-16-834G=
ENST00000688308.1:c.-17+507G= (PTEN) ENSP00000508752.1:n.-17+507G=
ENST00000692337.1:c.62G= (MLDHR) ENSP00000509326.1:p.Arg21=
ENST00000693560.1:c.-330G= (PTEN) ENSP00000509861.1:n.-330G=
ENST00000371953.7:c.-850G= (PTEN) ENSP00000361021.3:n.-850G=
ENST00000610634.1:c.-952G= (PTEN) ENSP00000477517.1:n.-952G=
NM_000314.5:c.-849G= (PTEN) NP_000305.3:n.-849G=
NM_000314.6:c.-849G= (PTEN) NP_000305.3:n.-849G=
NM_001304717.2:c.-330G= (PTEN) NP_001291646.2:n.-330G=
NM_001304718.1:c.-1554G= (PTEN) NP_001291647.1:n.-1554G=