Canonical Allele Identifier: CA1926143089

Gene: PTEN

Linked Data

• dbSNP Id: rs786204936

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87863546C>G , CM000672.2:g.87863546C>G	GRCh38
NC_000010.10:g.89623303C>G , CM000672.1:g.89623303C>G	GRCh37
NC_000010.9:g.89613283C>G	NCBI36
NG_007466.2:g.5109C>G , LRG_311:g.5109C>G
NG_033079.1:g.4892G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000706954.1:c.-17+904C>G	ENSP00000516674.1:n.-17+904C>G
ENST00000688308.1:c.-17+433C>G	ENSP00000508752.1:n.-17+433C>G
ENST00000693560.1:c.-404C>G	ENSP00000509861.1:n.-404C>G
ENST00000371953.7:c.-924C>G	ENSP00000361021.3:n.-924C>G
ENST00000610634.1:c.-1026C>G	ENSP00000477517.1:n.-1026C>G
NM_000314.5:c.-923C>G	NP_000305.3:n.-923C>G
NM_000314.6:c.-923C>G	NP_000305.3:n.-923C>G
NM_001304717.2:c.-404C>G	NP_001291646.2:n.-404C>G
NM_001304718.1:c.-1628C>G	NP_001291647.1:n.-1628C>G