Canonical Allele Identifier: CA211260859

Gene: PTEN

Linked Data

• dbSNP Id: rs1036771211
• gnomAD v3: 10-87967666-ATTG-A
• gnomAD v4: 10-87967666-ATTG-A
• MyVariant Identifiers: chr10:g.89727424_89727426del (hg19) ; chr10:g.87967667_87967669del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967669_87967671del , CM000672.2:g.87967669_87967671del	GRCh38
NC_000010.10:g.89727426_89727428del , CM000672.1:g.89727426_89727428del	GRCh37
NC_000010.9:g.89717406_89717408del	NCBI36
NG_007466.2:g.109231_109233del , LRG_311:g.109231_109233del

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*2438_*2440del	ENSP00000518161.1:n.*2438_*2440del
ENST00000688158.2:n.4144_4146del
ENST00000706954.1:c.*2197_*2199del	ENSP00000516674.1:n.*2197_*2199del
ENST00000706955.1:c.*3444_*3446del	ENSP00000516675.1:n.*3444_*3446del
ENST00000688158.1:c.*3520_*3522del	ENSP00000509254.1:n.*3520_*3522del
ENST00000693560.1:c.*2197_*2199del	ENSP00000509861.1:n.*2197_*2199del
ENST00000371953.8:c.*2197_*2199del MANE Select	ENSP00000361021.3:n.*2197_*2199del
ENST00000371953.7:c.*2197_*2199del	ENSP00000361021.3:n.*2197_*2199del
NM_000314.5:c.*2197_*2199del	NP_000305.3:n.*2197_*2199del
NM_000314.6:c.*2197_*2199del	NP_000305.3:n.*2197_*2199del
NM_001304717.2:c.*2197_*2199del	NP_001291646.2:n.*2197_*2199del
NM_001304718.1:c.*2197_*2199del	NP_001291647.1:n.*2197_*2199del
XM_006717926.2:c.*2197_*2199del	XP_006717989.1:n.*2197_*2199del
XM_011539982.1:c.*2197_*2199del	XP_011538284.1:n.*2197_*2199del
XR_945791.1:n.3979_3981del
NM_000314.7:c.*2197_*2199del	NP_000305.3:n.*2197_*2199del
NM_001304717.5:c.*2197_*2199del	NP_001291646.4:n.*2197_*2199del
NM_001304718.2:c.*2197_*2199del	NP_001291647.1:n.*2197_*2199del
NM_000314.8:c.*2197_*2199del MANE Select	NP_000305.3:n.*2197_*2199del