Canonical Allele Identifier: CA595184707

Gene: PTEN

Linked Data

• dbSNP Id: rs1429711809
• gnomAD v2: 10-89720955-TGAA-T
• gnomAD v3: 10-87961198-TGAA-T
• gnomAD v4: 10-87961198-TGAA-T
• MyVariant Identifiers: chr10:g.89720956_89720958del (hg19) ; chr10:g.87961199_87961201del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961202_87961204del , CM000672.2:g.87961202_87961204del	GRCh38
NC_000010.10:g.89720959_89720961del , CM000672.1:g.89720959_89720961del	GRCh37
NC_000010.9:g.89710939_89710941del	NCBI36
NG_007466.2:g.102764_102766del , LRG_311:g.102764_102766del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1119+84_1119+86del	ENSP00000514759.2:n.1119+84_1119+86del
ENST00000710265.1:c.1026+84_1026+86del	ENSP00000518161.1:n.1026+84_1026+86del
ENST00000472832.3:c.*75_*77del	ENSP00000483066.2:n.*75_*77del
ENST00000688158.2:n.1761+84_1761+86del
ENST00000688922.2:c.*856+84_*856+86del	ENSP00000508742.2:n.*856+84_*856+86del
ENST00000700021.1:c.981+84_981+86del	ENSP00000514757.1:n.981+84_981+86del
ENST00000700022.1:c.*365+84_*365+86del	ENSP00000514758.1:n.*365+84_*365+86del
ENST00000700023.1:n.2184+84_2184+86del
ENST00000700024.1:n.2418+84_2418+86del
ENST00000700025.1:n.1879_1881del
ENST00000700026.1:n.747_749del
ENST00000706954.1:c.1026+84_1026+86del	ENSP00000516674.1:n.1026+84_1026+86del
ENST00000706955.1:c.*1061+84_*1061+86del	ENSP00000516675.1:n.*1061+84_*1061+86del
ENST00000686459.1:c.*612+84_*612+86del	ENSP00000508909.1:n.*612+84_*612+86del
ENST00000688158.1:c.*1137+84_*1137+86del	ENSP00000509254.1:n.*1137+84_*1137+86del
ENST00000688308.1:c.1026+84_1026+86del	ENSP00000508752.1:n.1026+84_1026+86del
ENST00000688922.1:c.947+84_947+86del
ENST00000693560.1:c.1545+84_1545+86del	ENSP00000509861.1:n.1545+84_1545+86del
ENST00000371953.8:c.1026+84_1026+86del MANE Select	ENSP00000361021.3:n.1026+84_1026+86del
ENST00000371953.7:c.1026+84_1026+86del	ENSP00000361021.3:n.1026+84_1026+86del
ENST00000472832.2:c.537_539del	ENSP00000483066.1:n.537_539del
NM_000314.5:c.1026+84_1026+86del	NP_000305.3:n.1026+84_1026+86del
NM_000314.6:c.1026+84_1026+86del	NP_000305.3:n.1026+84_1026+86del
NM_001304717.2:c.1545+84_1545+86del	NP_001291646.2:n.1545+84_1545+86del
NM_001304718.1:c.435+84_435+86del	NP_001291647.1:n.435+84_435+86del
XM_006717926.2:c.981+84_981+86del	XP_006717989.1:n.981+84_981+86del
XM_011539981.1:c.1026+84_1026+86del	XP_011538283.1:n.1026+84_1026+86del
XM_011539982.1:c.930+84_930+86del	XP_011538284.1:n.930+84_930+86del
XR_945791.1:n.1596+84_1596+86del
NM_000314.7:c.1026+84_1026+86del	NP_000305.3:n.1026+84_1026+86del
NM_001304717.5:c.1545+84_1545+86del	NP_001291646.4:n.1545+84_1545+86del
NM_001304718.2:c.435+84_435+86del	NP_001291647.1:n.435+84_435+86del
NM_000314.8:c.1026+84_1026+86del MANE Select	NP_000305.3:n.1026+84_1026+86del