Canonical Allele Identifier: CA645580458

Gene: PTPN11

Linked Data

• COSMIC: COSM5611359

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112450395_112450396delinsTT , CM000674.2:g.112450395_112450396delinsTT	GRCh38
NC_000012.11:g.112888199_112888200delinsTT , CM000674.1:g.112888199_112888200delinsTT	GRCh37
NC_000012.10:g.111372582_111372583delinsTT	NCBI36
NG_007459.1:g.36664_36665delinsTT , LRG_614:g.36664_36665delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.215_216delinsTT	ENSP00000491593.2:p.Ala72Val
ENST00000685487.1:c.215_216delinsTT	ENSP00000508503.1:p.Ala72Val
ENST00000687906.1:c.215_216delinsTT	ENSP00000509536.1:p.Ala72Val
ENST00000688597.1:c.215_216delinsTT	ENSP00000510628.1:p.Ala72Val
ENST00000690210.1:c.215_216delinsTT	ENSP00000509272.1:p.Ala72Val
ENST00000692624.1:c.215_216delinsTT	ENSP00000508953.1:p.Ala72Val
ENST00000351677.7:c.215_216delinsTT MANE Select	ENSP00000340944.3:p.Ala72Val
ENST00000639857.1:c.215_216delinsTT	ENSP00000491593.1:p.Ala72Val
ENST00000351677.6:c.215_216delinsTT	ENSP00000340944.2:p.Ala72Val
ENST00000392597.5:c.215_216delinsTT	ENSP00000376376.1:p.Ala72Val
ENST00000635625.1:c.215_216delinsTT	ENSP00000489597.1:p.Ala72Val
NM_002834.3:c.215_216delinsTT , LRG_614t1:c.215_216delinsTT	NP_002825.3:p.Ala72Val
NM_080601.1:c.215_216delinsTT	NP_542168.1:p.Ala72Val
XM_006719526.1:c.215_216delinsTT	XP_006719589.1:p.Ala72Val
XM_006719527.1:c.215_216delinsTT	XP_006719590.1:p.Ala72Val
XM_011538613.1:c.212_213delinsTT	XP_011536915.1:p.Ala71Val
NM_001330437.1:c.215_216delinsTT	NP_001317366.1:p.Ala72Val
NM_002834.4:c.215_216delinsTT	NP_002825.3:p.Ala72Val
NM_080601.2:c.215_216delinsTT	NP_542168.1:p.Ala72Val
XM_011538613.2:c.212_213delinsTT	XP_011536915.1:p.Ala71Val
XM_017019722.1:c.212_213delinsTT	XP_016875211.1:p.Ala71Val
NM_001330437.2:c.215_216delinsTT	NP_001317366.1:p.Ala72Val
NM_001374625.1:c.212_213delinsTT	NP_001361554.1:p.Ala71Val
NM_002834.5:c.215_216delinsTT MANE Select	NP_002825.3:p.Ala72Val
NM_080601.3:c.215_216delinsTT	NP_542168.1:p.Ala72Val