Canonical Allele Identifier: CA2610046384

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863561G>A , CM000672.2:g.87863561G>A GRCh38
NC_000010.10:g.89623318G>A , CM000672.1:g.89623318G>A GRCh37
NC_000010.9:g.89613298G>A NCBI36
NG_007466.2:g.5124G>A , LRG_311:g.5124G>A
NG_033079.1:g.4877C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-893G>A (PTEN) ENSP00000516674.1:n.-16-893G>A
ENST00000688308.1:c.-17+448G>A (PTEN) ENSP00000508752.1:n.-17+448G>A
ENST00000692337.1:c.3G>A (MLDHR) ENSP00000509326.1:p.Met1Ile
ENST00000693560.1:c.-389G>A (PTEN) ENSP00000509861.1:n.-389G>A
ENST00000371953.7:c.-909G>A (PTEN) ENSP00000361021.3:n.-909G>A
ENST00000610634.1:c.-1011G>A (PTEN) ENSP00000477517.1:n.-1011G>A
NM_000314.5:c.-908G>A (PTEN) NP_000305.3:n.-908G>A
NM_000314.6:c.-908G>A (PTEN) NP_000305.3:n.-908G>A
NM_001304717.2:c.-389G>A (PTEN) NP_001291646.2:n.-389G>A
NM_001304718.1:c.-1613G>A (PTEN) NP_001291647.1:n.-1613G>A