Canonical Allele Identifier: CA1926143148

Linked Data

dbSNP Id: rs1348342875

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863612G>A , CM000672.2:g.87863612G>A GRCh38
NC_000010.10:g.89623369G>A , CM000672.1:g.89623369G>A GRCh37
NC_000010.9:g.89613349G>A NCBI36
NG_007466.2:g.5175G>A , LRG_311:g.5175G>A
NG_033079.1:g.4826C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-842G>A (PTEN) ENSP00000516674.1:n.-16-842G>A
ENST00000688308.1:c.-17+499G>A (PTEN) ENSP00000508752.1:n.-17+499G>A
ENST00000692337.1:c.54G>A (MLDHR) ENSP00000509326.1:p.Thr18=
ENST00000693560.1:c.-338G>A (PTEN) ENSP00000509861.1:n.-338G>A
ENST00000371953.7:c.-858G>A (PTEN) ENSP00000361021.3:n.-858G>A
ENST00000610634.1:c.-960G>A (PTEN) ENSP00000477517.1:n.-960G>A
NM_000314.5:c.-857G>A (PTEN) NP_000305.3:n.-857G>A
NM_000314.6:c.-857G>A (PTEN) NP_000305.3:n.-857G>A
NM_001304717.2:c.-338G>A (PTEN) NP_001291646.2:n.-338G>A
NM_001304718.1:c.-1562G>A (PTEN) NP_001291647.1:n.-1562G>A