Canonical Allele Identifier: CA2838032086

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863622T>G , CM000672.2:g.87863622T>G GRCh38
NC_000010.10:g.89623379T>G , CM000672.1:g.89623379T>G GRCh37
NC_000010.9:g.89613359T>G NCBI36
NG_007466.2:g.5185T>G , LRG_311:g.5185T>G
NG_033079.1:g.4816A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-832T>G (PTEN) ENSP00000516674.1:n.-16-832T>G
ENST00000688308.1:c.-17+509T>G (PTEN) ENSP00000508752.1:n.-17+509T>G
ENST00000692337.1:c.64T>G (MLDHR) ENSP00000509326.1:p.Ser22Ala
ENST00000693560.1:c.-328T>G (PTEN) ENSP00000509861.1:n.-328T>G
ENST00000371953.7:c.-848T>G (PTEN) ENSP00000361021.3:n.-848T>G
ENST00000610634.1:c.-950T>G (PTEN) ENSP00000477517.1:n.-950T>G
NM_000314.5:c.-847T>G (PTEN) NP_000305.3:n.-847T>G
NM_000314.6:c.-847T>G (PTEN) NP_000305.3:n.-847T>G
NM_001304717.2:c.-328T>G (PTEN) NP_001291646.2:n.-328T>G
NM_001304718.1:c.-1552T>G (PTEN) NP_001291647.1:n.-1552T>G