Canonical Allele Identifier: CA211260099

Gene: PTEN

Linked Data

• dbSNP Id: rs764649748
• gnomAD v3: 10-87966911-T-TG
• gnomAD v4: 10-87966911-T-TG
• MyVariant Identifiers: chr10:g.89726668_89726669insG (hg19) ; chr10:g.87966911_87966912insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966911_87966912insG , CM000672.2:g.87966911_87966912insG	GRCh38
NC_000010.10:g.89726668_89726669insG , CM000672.1:g.89726668_89726669insG	GRCh37
NC_000010.9:g.89716648_89716649insG	NCBI36
NG_007466.2:g.108473_108474insG , LRG_311:g.108473_108474insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1680_*1681insG	ENSP00000518161.1:n.*1680_*1681insG
ENST00000688158.2:n.3386_3387insG
ENST00000706954.1:c.*1439_*1440insG	ENSP00000516674.1:n.*1439_*1440insG
ENST00000706955.1:c.*2686_*2687insG	ENSP00000516675.1:n.*2686_*2687insG
ENST00000688158.1:c.*2762_*2763insG	ENSP00000509254.1:n.*2762_*2763insG
ENST00000693560.1:c.*1439_*1440insG	ENSP00000509861.1:n.*1439_*1440insG
ENST00000371953.8:c.*1439_*1440insG MANE Select	ENSP00000361021.3:n.*1439_*1440insG
ENST00000371953.7:c.*1439_*1440insG	ENSP00000361021.3:n.*1439_*1440insG
NM_000314.5:c.*1439_*1440insG	NP_000305.3:n.*1439_*1440insG
NM_000314.6:c.*1439_*1440insG	NP_000305.3:n.*1439_*1440insG
NM_001304717.2:c.*1439_*1440insG	NP_001291646.2:n.*1439_*1440insG
NM_001304718.1:c.*1439_*1440insG	NP_001291647.1:n.*1439_*1440insG
XM_006717926.2:c.*1439_*1440insG	XP_006717989.1:n.*1439_*1440insG
XM_011539982.1:c.*1439_*1440insG	XP_011538284.1:n.*1439_*1440insG
XR_945791.1:n.3221_3222insG
NM_000314.7:c.*1439_*1440insG	NP_000305.3:n.*1439_*1440insG
NM_001304717.5:c.*1439_*1440insG	NP_001291646.4:n.*1439_*1440insG
NM_001304718.2:c.*1439_*1440insG	NP_001291647.1:n.*1439_*1440insG
NM_000314.8:c.*1439_*1440insG MANE Select	NP_000305.3:n.*1439_*1440insG