Canonical Allele Identifier: CA2610046406

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863602G>A , CM000672.2:g.87863602G>A GRCh38
NC_000010.10:g.89623359G>A , CM000672.1:g.89623359G>A GRCh37
NC_000010.9:g.89613339G>A NCBI36
NG_007466.2:g.5165G>A , LRG_311:g.5165G>A
NG_033079.1:g.4836C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-852G>A (PTEN) ENSP00000516674.1:n.-16-852G>A
ENST00000688308.1:c.-17+489G>A (PTEN) ENSP00000508752.1:n.-17+489G>A
ENST00000692337.1:c.44G>A (MLDHR) ENSP00000509326.1:p.Gly15Asp
ENST00000693560.1:c.-348G>A (PTEN) ENSP00000509861.1:n.-348G>A
ENST00000371953.7:c.-868G>A (PTEN) ENSP00000361021.3:n.-868G>A
ENST00000610634.1:c.-970G>A (PTEN) ENSP00000477517.1:n.-970G>A
NM_000314.5:c.-867G>A (PTEN) NP_000305.3:n.-867G>A
NM_000314.6:c.-867G>A (PTEN) NP_000305.3:n.-867G>A
NM_001304717.2:c.-348G>A (PTEN) NP_001291646.2:n.-348G>A
NM_001304718.1:c.-1572G>A (PTEN) NP_001291647.1:n.-1572G>A