Canonical Allele Identifier: CA2610050012

Gene: PTEN

Linked Data

• gnomAD v4: 10-87967738-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967743del , CM000672.2:g.87967743del	GRCh38
NC_000010.10:g.89727500del , CM000672.1:g.89727500del	GRCh37
NC_000010.9:g.89717480del	NCBI36
NG_007466.2:g.109305del , LRG_311:g.109305del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*2512del	ENSP00000518161.1:n.*2512del
ENST00000688158.2:n.4218del
ENST00000706954.1:c.*2271del	ENSP00000516674.1:n.*2271del
ENST00000706955.1:c.*3518del	ENSP00000516675.1:n.*3518del
ENST00000688158.1:c.*3594del	ENSP00000509254.1:n.*3594del
ENST00000693560.1:c.*2271del	ENSP00000509861.1:n.*2271del
ENST00000371953.8:c.*2271del MANE Select	ENSP00000361021.3:n.*2271del
ENST00000371953.7:c.*2271del	ENSP00000361021.3:n.*2271del
NM_000314.5:c.*2271del	NP_000305.3:n.*2271del
NM_000314.6:c.*2271del	NP_000305.3:n.*2271del
NM_001304717.2:c.*2271del	NP_001291646.2:n.*2271del
NM_001304718.1:c.*2271del	NP_001291647.1:n.*2271del
XM_006717926.2:c.*2271del	XP_006717989.1:n.*2271del
XM_011539982.1:c.*2271del	XP_011538284.1:n.*2271del
XR_945791.1:n.4053del
NM_000314.7:c.*2271del	NP_000305.3:n.*2271del
NM_001304717.5:c.*2271del	NP_001291646.4:n.*2271del
NM_001304718.2:c.*2271del	NP_001291647.1:n.*2271del
NM_000314.8:c.*2271del MANE Select	NP_000305.3:n.*2271del