Canonical Allele Identifier: CA2063775849
Gene: PTPN11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.112477766_112477767delinsCA , CM000674.2:g.112477766_112477767delinsCA GRCh38
NC_000012.11:g.112915570_112915571delinsCA , CM000674.1:g.112915570_112915571delinsCA GRCh37
NC_000012.10:g.111399953_111399954delinsCA NCBI36
NG_007459.1:g.64035_64036delinsCA , LRG_614:g.64035_64036delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000639857.2:c.933+36_933+37delinsCA ENSP00000491593.2:n.933+36_933+37delinsCA
ENST00000685487.1:c.933+36_933+37delinsCA ENSP00000508503.1:n.933+36_933+37delinsCA
ENST00000687906.1:c.819+36_819+37delinsCA ENSP00000509536.1:n.819+36_819+37delinsCA
ENST00000688597.1:c.933+36_933+37delinsCA ENSP00000510628.1:n.933+36_933+37delinsCA
ENST00000690210.1:c.933+36_933+37delinsCA ENSP00000509272.1:n.933+36_933+37delinsCA
ENST00000692624.1:c.933+36_933+37delinsCA ENSP00000508953.1:n.933+36_933+37delinsCA
ENST00000351677.7:c.933+36_933+37delinsCA MANE Select ENSP00000340944.3:n.933+36_933+37delinsCA
ENST00000351677.6:c.933+36_933+37delinsCA ENSP00000340944.2:n.933+36_933+37delinsCA
ENST00000392597.5:c.933+36_933+37delinsCA ENSP00000376376.1:n.933+36_933+37delinsCA
ENST00000635625.1:c.933+36_933+37delinsCA ENSP00000489597.1:n.933+36_933+37delinsCA
NM_002834.3:c.933+36_933+37delinsCA , LRG_614t1:c.933+36_933+37delinsCA NP_002825.3:n.933+36_933+37delinsCA
NM_080601.1:c.933+36_933+37delinsCA NP_542168.1:n.933+36_933+37delinsCA
XM_006719526.1:c.933+36_933+37delinsCA XP_006719589.1:n.933+36_933+37delinsCA
XM_006719527.1:c.819+36_819+37delinsCA XP_006719590.1:n.819+36_819+37delinsCA
XM_011538613.1:c.930+36_930+37delinsCA XP_011536915.1:n.930+36_930+37delinsCA
NM_001330437.1:c.933+36_933+37delinsCA NP_001317366.1:n.933+36_933+37delinsCA
NM_002834.4:c.933+36_933+37delinsCA NP_002825.3:n.933+36_933+37delinsCA
NM_080601.2:c.933+36_933+37delinsCA NP_542168.1:n.933+36_933+37delinsCA
XM_011538613.2:c.930+36_930+37delinsCA XP_011536915.1:n.930+36_930+37delinsCA
XM_017019722.1:c.930+36_930+37delinsCA XP_016875211.1:n.930+36_930+37delinsCA
NM_001330437.2:c.933+36_933+37delinsCA NP_001317366.1:n.933+36_933+37delinsCA
NM_001374625.1:c.930+36_930+37delinsCA NP_001361554.1:n.930+36_930+37delinsCA
NM_002834.5:c.933+36_933+37delinsCA MANE Select NP_002825.3:n.933+36_933+37delinsCA
NM_080601.3:c.933+36_933+37delinsCA NP_542168.1:n.933+36_933+37delinsCA