Canonical Allele Identifier: CA2727226228
Gene: PTPN11 HGNC NCBI

Linked Data

dbSNP Id: rs2135901866

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.112477897del , CM000674.2:g.112477897del GRCh38
NC_000012.11:g.112915701del , CM000674.1:g.112915701del GRCh37
NC_000012.10:g.111400084del NCBI36
NG_007459.1:g.64166del , LRG_614:g.64166del

Transcript Alleles

HGVS Amino-acid change
ENST00000639857.2:c.974del ENSP00000491593.2:p.Lys325ArgfsTer14
ENST00000685487.1:c.974del ENSP00000508503.1:p.Lys325ArgfsTer14
ENST00000687906.1:c.860del ENSP00000509536.1:p.Lys287ArgfsTer14
ENST00000688597.1:c.974del ENSP00000510628.1:p.Lys325ArgfsTer14
ENST00000690210.1:c.974del ENSP00000509272.1:p.Lys325ArgfsTer14
ENST00000692624.1:c.974del ENSP00000508953.1:p.Lys325ArgfsTer14
ENST00000351677.7:c.974del MANE Select ENSP00000340944.3:p.Lys325ArgfsTer14
ENST00000351677.6:c.974del ENSP00000340944.2:p.Lys325ArgfsTer14
ENST00000392597.5:c.974del ENSP00000376376.1:p.Lys325ArgfsTer14
ENST00000635625.1:c.974del ENSP00000489597.1:p.Lys325ArgfsTer14
NM_002834.3:c.974del , LRG_614t1:c.974del NP_002825.3:p.Lys325ArgfsTer14
NM_080601.1:c.974del NP_542168.1:p.Lys325ArgfsTer14
XM_006719526.1:c.974del XP_006719589.1:p.Lys325ArgfsTer14
XM_006719527.1:c.860del XP_006719590.1:p.Lys287ArgfsTer14
XM_011538613.1:c.971del XP_011536915.1:p.Lys324ArgfsTer14
NM_001330437.1:c.974del NP_001317366.1:p.Lys325ArgfsTer14
NM_002834.4:c.974del NP_002825.3:p.Lys325ArgfsTer14
NM_080601.2:c.974del NP_542168.1:p.Lys325ArgfsTer14
XM_011538613.2:c.971del XP_011536915.1:p.Lys324ArgfsTer14
XM_017019722.1:c.971del XP_016875211.1:p.Lys324ArgfsTer14
NM_001330437.2:c.974del NP_001317366.1:p.Lys325ArgfsTer14
NM_001374625.1:c.971del NP_001361554.1:p.Lys324ArgfsTer14
NM_002834.5:c.974del MANE Select NP_002825.3:p.Lys325ArgfsTer14
NM_080601.3:c.974del NP_542168.1:p.Lys325ArgfsTer14