Canonical Allele Identifier: CA211260358

Gene: PTEN

Linked Data

• dbSNP Id: rs201650436
• gnomAD v2: 10-89726860-G-GT
• gnomAD v3: 10-87967103-G-GT
• gnomAD v4: 10-87967103-G-GT
• MyVariant Identifiers: chr10:g.89726860_89726861insT (hg19) ; chr10:g.87967103_87967104insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967112dup , CM000672.2:g.87967112dup	GRCh38
NC_000010.10:g.89726869dup , CM000672.1:g.89726869dup	GRCh37
NC_000010.9:g.89716849dup	NCBI36
NG_007466.2:g.108674dup , LRG_311:g.108674dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1881dup	ENSP00000518161.1:n.*1881dup
ENST00000688158.2:n.3587dup
ENST00000706954.1:c.*1640dup	ENSP00000516674.1:n.*1640dup
ENST00000706955.1:c.*2887dup	ENSP00000516675.1:n.*2887dup
ENST00000688158.1:c.*2963dup	ENSP00000509254.1:n.*2963dup
ENST00000693560.1:c.*1640dup	ENSP00000509861.1:n.*1640dup
ENST00000371953.8:c.*1640dup MANE Select	ENSP00000361021.3:n.*1640dup
ENST00000371953.7:c.*1640dup	ENSP00000361021.3:n.*1640dup
NM_000314.5:c.*1640dup	NP_000305.3:n.*1640dup
NM_000314.6:c.*1640dup	NP_000305.3:n.*1640dup
NM_001304717.2:c.*1640dup	NP_001291646.2:n.*1640dup
NM_001304718.1:c.*1640dup	NP_001291647.1:n.*1640dup
XM_006717926.2:c.*1640dup	XP_006717989.1:n.*1640dup
XM_011539982.1:c.*1640dup	XP_011538284.1:n.*1640dup
XR_945791.1:n.3422dup
NM_000314.7:c.*1640dup	NP_000305.3:n.*1640dup
NM_001304717.5:c.*1640dup	NP_001291646.4:n.*1640dup
NM_001304718.2:c.*1640dup	NP_001291647.1:n.*1640dup
NM_000314.8:c.*1640dup MANE Select	NP_000305.3:n.*1640dup