Canonical Allele Identifier: CA669574303

Gene: PTEN

Linked Data

• dbSNP Id: rs5786797
• gnomAD v3: 10-87966902-G-GTTTT
• gnomAD v4: 10-87966902-G-GTTTT
• MyVariant Identifiers: chr10:g.87966902_87966903insTTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966928_87966931dup , CM000672.2:g.87966928_87966931dup	GRCh38
NC_000010.10:g.89726685_89726688dup , CM000672.1:g.89726685_89726688dup	GRCh37
NC_000010.9:g.89716665_89716668dup	NCBI36
NG_007466.2:g.108490_108493dup , LRG_311:g.108490_108493dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*1697_*1700dup	ENSP00000518161.1:n.*1697_*1700dup
ENST00000688158.2:n.3403_3406dup
ENST00000706954.1:c.*1456_*1459dup	ENSP00000516674.1:n.*1456_*1459dup
ENST00000706955.1:c.*2703_*2706dup	ENSP00000516675.1:n.*2703_*2706dup
ENST00000688158.1:c.*2779_*2782dup	ENSP00000509254.1:n.*2779_*2782dup
ENST00000693560.1:c.*1456_*1459dup	ENSP00000509861.1:n.*1456_*1459dup
ENST00000371953.8:c.*1456_*1459dup MANE Select	ENSP00000361021.3:n.*1456_*1459dup
ENST00000371953.7:c.*1456_*1459dup	ENSP00000361021.3:n.*1456_*1459dup
NM_000314.5:c.*1456_*1459dup	NP_000305.3:n.*1456_*1459dup
NM_000314.6:c.*1456_*1459dup	NP_000305.3:n.*1456_*1459dup
NM_001304717.2:c.*1456_*1459dup	NP_001291646.2:n.*1456_*1459dup
NM_001304718.1:c.*1456_*1459dup	NP_001291647.1:n.*1456_*1459dup
XM_006717926.2:c.*1456_*1459dup	XP_006717989.1:n.*1456_*1459dup
XM_011539982.1:c.*1456_*1459dup	XP_011538284.1:n.*1456_*1459dup
XR_945791.1:n.3238_3241dup
NM_000314.7:c.*1456_*1459dup	NP_000305.3:n.*1456_*1459dup
NM_001304717.5:c.*1456_*1459dup	NP_001291646.4:n.*1456_*1459dup
NM_001304718.2:c.*1456_*1459dup	NP_001291647.1:n.*1456_*1459dup
NM_000314.8:c.*1456_*1459dup MANE Select	NP_000305.3:n.*1456_*1459dup