Canonical Allele Identifier: CA1926177669

Gene: PTEN

Linked Data

• dbSNP Id: rs1860813297

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87968023_87968034del , CM000672.2:g.87968023_87968034del	GRCh38
NC_000010.10:g.89727780_89727791del , CM000672.1:g.89727780_89727791del	GRCh37
NC_000010.9:g.89717760_89717771del	NCBI36
NG_007466.2:g.109585_109596del , LRG_311:g.109585_109596del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*2792_*2803del	ENSP00000518161.1:n.*2792_*2803del
ENST00000688158.2:n.4498_4509del
ENST00000706954.1:c.*2551_*2562del	ENSP00000516674.1:n.*2551_*2562del
ENST00000706955.1:c.*3798_*3809del	ENSP00000516675.1:n.*3798_*3809del
ENST00000688158.1:c.*3874_*3885del	ENSP00000509254.1:n.*3874_*3885del
ENST00000693560.1:c.*2551_*2562del	ENSP00000509861.1:n.*2551_*2562del
ENST00000371953.8:c.*2551_*2562del MANE Select	ENSP00000361021.3:n.*2551_*2562del
ENST00000371953.7:c.*2551_*2562del	ENSP00000361021.3:n.*2551_*2562del
NM_000314.5:c.*2551_*2562del	NP_000305.3:n.*2551_*2562del
NM_000314.6:c.*2551_*2562del	NP_000305.3:n.*2551_*2562del
NM_001304717.2:c.*2551_*2562del	NP_001291646.2:n.*2551_*2562del
NM_001304718.1:c.*2551_*2562del	NP_001291647.1:n.*2551_*2562del
XM_006717926.2:c.*2551_*2562del	XP_006717989.1:n.*2551_*2562del
XM_011539982.1:c.*2551_*2562del	XP_011538284.1:n.*2551_*2562del
XR_945791.1:n.4333_4344del
NM_000314.7:c.*2551_*2562del	NP_000305.3:n.*2551_*2562del
NM_001304717.5:c.*2551_*2562del	NP_001291646.4:n.*2551_*2562del
NM_001304718.2:c.*2551_*2562del	NP_001291647.1:n.*2551_*2562del
NM_000314.8:c.*2551_*2562del MANE Select	NP_000305.3:n.*2551_*2562del