Canonical Allele Identifier: CA1926177033

Gene: PTEN

Linked Data

• dbSNP Id: rs1860802694

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967621_87967623del , CM000672.2:g.87967621_87967623del	GRCh38
NC_000010.10:g.89727378_89727380del , CM000672.1:g.89727378_89727380del	GRCh37
NC_000010.9:g.89717358_89717360del	NCBI36
NG_007466.2:g.109183_109185del , LRG_311:g.109183_109185del

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*2390_*2392del	ENSP00000518161.1:n.*2390_*2392del
ENST00000688158.2:n.4096_4098del
ENST00000706954.1:c.*2149_*2151del	ENSP00000516674.1:n.*2149_*2151del
ENST00000706955.1:c.*3396_*3398del	ENSP00000516675.1:n.*3396_*3398del
ENST00000688158.1:c.*3472_*3474del	ENSP00000509254.1:n.*3472_*3474del
ENST00000693560.1:c.*2149_*2151del	ENSP00000509861.1:n.*2149_*2151del
ENST00000371953.8:c.*2149_*2151del MANE Select	ENSP00000361021.3:n.*2149_*2151del
ENST00000371953.7:c.*2149_*2151del	ENSP00000361021.3:n.*2149_*2151del
NM_000314.5:c.*2149_*2151del	NP_000305.3:n.*2149_*2151del
NM_000314.6:c.*2149_*2151del	NP_000305.3:n.*2149_*2151del
NM_001304717.2:c.*2149_*2151del	NP_001291646.2:n.*2149_*2151del
NM_001304718.1:c.*2149_*2151del	NP_001291647.1:n.*2149_*2151del
XM_006717926.2:c.*2149_*2151del	XP_006717989.1:n.*2149_*2151del
XM_011539982.1:c.*2149_*2151del	XP_011538284.1:n.*2149_*2151del
XR_945791.1:n.3931_3933del
NM_000314.7:c.*2149_*2151del	NP_000305.3:n.*2149_*2151del
NM_001304717.5:c.*2149_*2151del	NP_001291646.4:n.*2149_*2151del
NM_001304718.2:c.*2149_*2151del	NP_001291647.1:n.*2149_*2151del
NM_000314.8:c.*2149_*2151del MANE Select	NP_000305.3:n.*2149_*2151del