Canonical Allele Identifier: CA2063740642

Gene: PTPN11

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112488948_112488992delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT , CM000674.2:g.112488948_112488992delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	GRCh38
NC_000012.11:g.112926752_112926796delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT , CM000674.1:g.112926752_112926796delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	GRCh37
NC_000012.10:g.111411135_111411179delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	NCBI36
NG_007459.1:g.75217_75261delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT , LRG_614:g.75217_75261delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000639857.2:c.1448-76_1448-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	ENSP00000491593.2:n.1448-76_1448-32delins...
ENST00000685487.1:c.1448-76_1448-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	ENSP00000508503.1:n.1448-76_1448-32delins...
ENST00000687624.1:n.113-76_113-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT
ENST00000687906.1:c.1334-76_1334-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	ENSP00000509536.1:n.1334-76_1334-32delins...
ENST00000688597.1:c.1224+6743_1224+6787delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	ENSP00000510628.1:n.1224+6743_1224+6787de...
ENST00000688701.1:n.692-76_692-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT
ENST00000690210.1:c.1448-76_1448-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	ENSP00000509272.1:n.1448-76_1448-32delins...
ENST00000690472.1:n.657-76_657-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT
ENST00000692624.1:c.1380-76_1380-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	ENSP00000508953.1:n.1380-76_1380-32delins...
ENST00000351677.7:c.1448-76_1448-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT MANE Select	ENSP00000340944.3:n.1448-76_1448-32delins...
ENST00000351677.6:c.1448-76_1448-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	ENSP00000340944.2:n.1448-76_1448-32delins...
ENST00000635625.1:c.1460-76_1460-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	ENSP00000489597.1:n.1460-76_1460-32delins...
ENST00000635652.1:c.461-76_461-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	ENSP00000489541.1:n.461-76_461-32delinsAC...
NM_002834.3:c.1448-76_1448-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT , LRG_614t1:c.1448-76_1448-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	NP_002825.3:n.1448-76_1448-32delinsACTAAA...
XM_006719526.1:c.1460-76_1460-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	XP_006719589.1:n.1460-76_1460-32delinsACT...
XM_006719527.1:c.1346-76_1346-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	XP_006719590.1:n.1346-76_1346-32delinsACT...
XM_011538613.1:c.1457-76_1457-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	XP_011536915.1:n.1457-76_1457-32delinsACT...
NM_001330437.1:c.1460-76_1460-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	NP_001317366.1:n.1460-76_1460-32delinsACT...
NM_002834.4:c.1448-76_1448-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	NP_002825.3:n.1448-76_1448-32delinsACTAAA...
XM_011538613.2:c.1457-76_1457-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	XP_011536915.1:n.1457-76_1457-32delinsACT...
XM_017019722.1:c.1445-76_1445-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	XP_016875211.1:n.1445-76_1445-32delinsACT...
NM_001330437.2:c.1460-76_1460-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	NP_001317366.1:n.1460-76_1460-32delinsACT...
NM_001374625.1:c.1445-76_1445-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT	NP_001361554.1:n.1445-76_1445-32delinsACT...
NM_002834.5:c.1448-76_1448-32delinsACTAAAAGTTGTGCATTAAACAACTTCATCCTGGCTCTGCAGTTT MANE Select	NP_002825.3:n.1448-76_1448-32delinsACTAAA...