Canonical Allele Identifier: CA669574839

Gene: PTEN

Linked Data

• dbSNP Id: rs1368243421
• gnomAD v3: 10-87967380-GTCAGTT-G
• gnomAD v4: 10-87967380-GTCAGTT-G
• MyVariant Identifiers: chr10:g.87967381_87967386del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967384_87967389del , CM000672.2:g.87967384_87967389del	GRCh38
NC_000010.10:g.89727141_89727146del , CM000672.1:g.89727141_89727146del	GRCh37
NC_000010.9:g.89717121_89717126del	NCBI36
NG_007466.2:g.108946_108951del , LRG_311:g.108946_108951del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*2153_*2158del	ENSP00000518161.1:n.*2153_*2158del
ENST00000688158.2:n.3859_3864del
ENST00000706954.1:c.*1912_*1917del	ENSP00000516674.1:n.*1912_*1917del
ENST00000706955.1:c.*3159_*3164del	ENSP00000516675.1:n.*3159_*3164del
ENST00000688158.1:c.*3235_*3240del	ENSP00000509254.1:n.*3235_*3240del
ENST00000693560.1:c.*1912_*1917del	ENSP00000509861.1:n.*1912_*1917del
ENST00000371953.8:c.*1912_*1917del MANE Select	ENSP00000361021.3:n.*1912_*1917del
ENST00000371953.7:c.*1912_*1917del	ENSP00000361021.3:n.*1912_*1917del
NM_000314.5:c.*1912_*1917del	NP_000305.3:n.*1912_*1917del
NM_000314.6:c.*1912_*1917del	NP_000305.3:n.*1912_*1917del
NM_001304717.2:c.*1912_*1917del	NP_001291646.2:n.*1912_*1917del
NM_001304718.1:c.*1912_*1917del	NP_001291647.1:n.*1912_*1917del
XM_006717926.2:c.*1912_*1917del	XP_006717989.1:n.*1912_*1917del
XM_011539982.1:c.*1912_*1917del	XP_011538284.1:n.*1912_*1917del
XR_945791.1:n.3694_3699del
NM_000314.7:c.*1912_*1917del	NP_000305.3:n.*1912_*1917del
NM_001304717.5:c.*1912_*1917del	NP_001291646.4:n.*1912_*1917del
NM_001304718.2:c.*1912_*1917del	NP_001291647.1:n.*1912_*1917del
NM_000314.8:c.*1912_*1917del MANE Select	NP_000305.3:n.*1912_*1917del