Canonical Allele Identifier: CA655001854

Gene: PTPN11

Linked Data

• COSMIC: COSN14845190

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112507247_112507248insT , CM000674.2:g.112507247_112507248insT	GRCh38
NC_000012.11:g.112945051_112945052insT , CM000674.1:g.112945051_112945052insT	GRCh37
NC_000012.10:g.111429434_111429435insT	NCBI36
NG_007459.1:g.93516_93517insT , LRG_614:g.93516_93517insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000639857.2:c.*1398_*1399insT	ENSP00000491593.2:n.*1398_*1399insT
ENST00000685487.1:c.*2439_*2440insT	ENSP00000508503.1:n.*2439_*2440insT
ENST00000687120.1:n.5058_5059insT
ENST00000687906.1:c.*1455_*1456insT	ENSP00000509536.1:n.*1455_*1456insT
ENST00000688597.1:c.*1455_*1456insT	ENSP00000510628.1:n.*1455_*1456insT
ENST00000688701.1:n.2481_2482insT
ENST00000690210.1:c.*1455_*1456insT	ENSP00000509272.1:n.*1455_*1456insT
ENST00000690472.1:n.2446_2447insT
ENST00000692624.1:c.*1783_*1784insT	ENSP00000508953.1:n.*1783_*1784insT
ENST00000351677.7:c.*1455_*1456insT MANE Select	ENSP00000340944.3:n.*1455_*1456insT
ENST00000351677.6:c.*1455_*1456insT	ENSP00000340944.2:n.*1455_*1456insT
NM_002834.3:c.*1455_*1456insT , LRG_614t1:c.*1455_*1456insT	NP_002825.3:n.*1455_*1456insT
XM_006719526.1:c.*1455_*1456insT	XP_006719589.1:n.*1455_*1456insT
XM_006719527.1:c.*1455_*1456insT	XP_006719590.1:n.*1455_*1456insT
XM_011538613.1:c.*1455_*1456insT	XP_011536915.1:n.*1455_*1456insT
NM_001330437.1:c.*1455_*1456insT	NP_001317366.1:n.*1455_*1456insT
NM_002834.4:c.*1455_*1456insT	NP_002825.3:n.*1455_*1456insT
XM_011538613.2:c.*1455_*1456insT	XP_011536915.1:n.*1455_*1456insT
XM_017019722.1:c.*1455_*1456insT	XP_016875211.1:n.*1455_*1456insT
NM_001330437.2:c.*1455_*1456insT	NP_001317366.1:n.*1455_*1456insT
NM_001374625.1:c.*1455_*1456insT	NP_001361554.1:n.*1455_*1456insT
NM_002834.5:c.*1455_*1456insT MANE Select	NP_002825.3:n.*1455_*1456insT