Canonical Allele Identifier: CA2722434711

Gene: PTEN

Linked Data

• dbSNP Id: rs2132278065

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87958082del , CM000672.2:g.87958082del	GRCh38
NC_000010.10:g.89717839del , CM000672.1:g.89717839del	GRCh37
NC_000010.9:g.89707819del	NCBI36
NG_007466.2:g.99644del , LRG_311:g.99644del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.801+63del	ENSP00000514759.2:n.801+63del
ENST00000710265.1:c.801+63del	ENSP00000518161.1:n.801+63del
ENST00000472832.3:c.801+63del	ENSP00000483066.2:n.801+63del
ENST00000688158.2:n.1536+63del
ENST00000688922.2:c.*631+63del	ENSP00000508742.2:n.*631+63del
ENST00000700021.1:c.756+63del	ENSP00000514757.1:n.756+63del
ENST00000700022.1:c.*140+63del	ENSP00000514758.1:n.*140+63del
ENST00000700023.1:n.1959+63del
ENST00000700024.1:n.2193+63del
ENST00000700025.1:n.1570+63del
ENST00000700026.1:n.438+63del
ENST00000700029.1:c.635+63del
ENST00000706954.1:c.801+63del	ENSP00000516674.1:n.801+63del
ENST00000706955.1:c.*836+63del	ENSP00000516675.1:n.*836+63del
ENST00000686459.1:c.*387+63del	ENSP00000508909.1:n.*387+63del
ENST00000688158.1:c.*912+63del	ENSP00000509254.1:n.*912+63del
ENST00000688308.1:c.801+63del	ENSP00000508752.1:n.801+63del
ENST00000688922.1:c.722+63del
ENST00000693560.1:c.1320+63del	ENSP00000509861.1:n.1320+63del
ENST00000371953.8:c.801+63del MANE Select	ENSP00000361021.3:n.801+63del
ENST00000371953.7:c.801+63del	ENSP00000361021.3:n.801+63del
ENST00000472832.2:c.228+63del	ENSP00000483066.1:n.228+63del
NM_000314.5:c.801+63del	NP_000305.3:n.801+63del
NM_000314.6:c.801+63del	NP_000305.3:n.801+63del
NM_001304717.2:c.1320+63del	NP_001291646.2:n.1320+63del
NM_001304718.1:c.210+63del	NP_001291647.1:n.210+63del
XM_006717926.2:c.756+63del	XP_006717989.1:n.756+63del
XM_011539981.1:c.801+63del	XP_011538283.1:n.801+63del
XM_011539982.1:c.705+63del	XP_011538284.1:n.705+63del
XR_945791.1:n.1371+63del
NM_000314.7:c.801+63del	NP_000305.3:n.801+63del
NM_001304717.5:c.1320+63del	NP_001291646.4:n.1320+63del
NM_001304718.2:c.210+63del	NP_001291647.1:n.210+63del
NM_000314.8:c.801+63del MANE Select	NP_000305.3:n.801+63del