Canonical Allele Identifier: CA2722366918

Gene: PTEN

Linked Data

• dbSNP Id: rs1554893737

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894006C>G , CM000672.2:g.87894006C>G	GRCh38
NC_000010.10:g.89653763C>G , CM000672.1:g.89653763C>G	GRCh37
NC_000010.9:g.89643743C>G	NCBI36
NG_007466.2:g.35568C>G , LRG_311:g.35568C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.80-19C>G	ENSP00000514759.2:n.80-19C>G
ENST00000710265.1:c.80-19C>G	ENSP00000518161.1:n.80-19C>G
ENST00000472832.3:c.80-19C>G	ENSP00000483066.2:n.80-19C>G
ENST00000688158.2:n.899+13568C>G
ENST00000688922.2:c.80-19C>G	ENSP00000508742.2:n.80-19C>G
ENST00000700021.1:c.80-19C>G	ENSP00000514757.1:n.80-19C>G
ENST00000700022.1:c.80-19C>G	ENSP00000514758.1:n.80-19C>G
ENST00000706954.1:c.80-19C>G	ENSP00000516674.1:n.80-19C>G
ENST00000706955.1:c.*115-19C>G	ENSP00000516675.1:n.*115-19C>G
ENST00000686459.1:c.80-19C>G	ENSP00000508909.1:n.80-19C>G
ENST00000688158.1:c.*275+13568C>G	ENSP00000509254.1:n.*275+13568C>G
ENST00000688308.1:c.80-19C>G	ENSP00000508752.1:n.80-19C>G
ENST00000693560.1:c.599-19C>G	ENSP00000509861.1:n.599-19C>G
ENST00000371953.8:c.80-19C>G MANE Select	ENSP00000361021.3:n.80-19C>G
ENST00000371953.7:c.80-19C>G	ENSP00000361021.3:n.80-19C>G
ENST00000462694.1:n.82-19C>G
ENST00000610634.1:c.-23-19C>G	ENSP00000477517.1:n.-23-19C>G
NM_000314.5:c.80-19C>G	NP_000305.3:n.80-19C>G
NM_000314.6:c.80-19C>G	NP_000305.3:n.80-19C>G
NM_001304717.2:c.599-19C>G	NP_001291646.2:n.599-19C>G
NM_001304718.1:c.-626-19C>G	NP_001291647.1:n.-626-19C>G
XM_006717926.2:c.80-19C>G	XP_006717989.1:n.80-19C>G
XM_011539981.1:c.80-19C>G	XP_011538283.1:n.80-19C>G
XM_011539982.1:c.68+13568C>G	XP_011538284.1:n.68+13568C>G
XR_945789.1:n.792-19C>G
XR_945790.1:n.792-19C>G
XR_945791.1:n.792-19C>G
NM_000314.7:c.80-19C>G	NP_000305.3:n.80-19C>G
NM_001304717.5:c.599-19C>G	NP_001291646.4:n.599-19C>G
NM_001304718.2:c.-626-19C>G	NP_001291647.1:n.-626-19C>G
NM_000314.8:c.80-19C>G MANE Select	NP_000305.3:n.80-19C>G