Canonical Allele Identifier: CA1926143080

Gene: PTEN

Linked Data

• dbSNP Id: rs889785939

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87863537G>T , CM000672.2:g.87863537G>T	GRCh38
NC_000010.10:g.89623294G>T , CM000672.1:g.89623294G>T	GRCh37
NC_000010.9:g.89613274G>T	NCBI36
NG_007466.2:g.5100G>T , LRG_311:g.5100G>T
NG_033079.1:g.4901C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706954.1:c.-17+895G>T	ENSP00000516674.1:n.-17+895G>T
ENST00000688308.1:c.-17+424G>T	ENSP00000508752.1:n.-17+424G>T
ENST00000693560.1:c.-413G>T	ENSP00000509861.1:n.-413G>T
ENST00000371953.7:c.-933G>T	ENSP00000361021.3:n.-933G>T
ENST00000610634.1:c.-1035G>T	ENSP00000477517.1:n.-1035G>T
NM_000314.5:c.-932G>T	NP_000305.3:n.-932G>T
NM_000314.6:c.-932G>T	NP_000305.3:n.-932G>T
NM_001304717.2:c.-413G>T	NP_001291646.2:n.-413G>T
NM_001304718.1:c.-1637G>T	NP_001291647.1:n.-1637G>T