Canonical Allele Identifier: CA2610049967

Gene: PTEN

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967579_87967580del , CM000672.2:g.87967579_87967580del	GRCh38
NC_000010.10:g.89727336_89727337del , CM000672.1:g.89727336_89727337del	GRCh37
NC_000010.9:g.89717316_89717317del	NCBI36
NG_007466.2:g.109141_109142del , LRG_311:g.109141_109142del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*2348_*2349del	ENSP00000518161.1:n.*2348_*2349del
ENST00000688158.2:n.4054_4055del
ENST00000706954.1:c.*2107_*2108del	ENSP00000516674.1:n.*2107_*2108del
ENST00000706955.1:c.*3354_*3355del	ENSP00000516675.1:n.*3354_*3355del
ENST00000688158.1:c.*3430_*3431del	ENSP00000509254.1:n.*3430_*3431del
ENST00000693560.1:c.*2107_*2108del	ENSP00000509861.1:n.*2107_*2108del
ENST00000371953.8:c.*2107_*2108del MANE Select	ENSP00000361021.3:n.*2107_*2108del
ENST00000371953.7:c.*2107_*2108del	ENSP00000361021.3:n.*2107_*2108del
NM_000314.5:c.*2107_*2108del	NP_000305.3:n.*2107_*2108del
NM_000314.6:c.*2107_*2108del	NP_000305.3:n.*2107_*2108del
NM_001304717.2:c.*2107_*2108del	NP_001291646.2:n.*2107_*2108del
NM_001304718.1:c.*2107_*2108del	NP_001291647.1:n.*2107_*2108del
XM_006717926.2:c.*2107_*2108del	XP_006717989.1:n.*2107_*2108del
XM_011539982.1:c.*2107_*2108del	XP_011538284.1:n.*2107_*2108del
XR_945791.1:n.3889_3890del
NM_000314.7:c.*2107_*2108del	NP_000305.3:n.*2107_*2108del
NM_001304717.5:c.*2107_*2108del	NP_001291646.4:n.*2107_*2108del
NM_001304718.2:c.*2107_*2108del	NP_001291647.1:n.*2107_*2108del
NM_000314.8:c.*2107_*2108del MANE Select	NP_000305.3:n.*2107_*2108del