Canonical Allele Identifier: CA134659
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 36708
dbSNP Id: rs61736914

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.112450435C>T , CM000674.2:g.112450435C>T GRCh38
NC_000012.11:g.112888239C>T , CM000674.1:g.112888239C>T GRCh37
NC_000012.10:g.111372622C>T NCBI36
NG_007459.1:g.36704C>T , LRG_614:g.36704C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000639857.2:c.255C>T ENSP00000491593.2:p.His85=
ENST00000685487.1:c.255C>T ENSP00000508503.1:p.His85=
ENST00000687906.1:c.255C>T ENSP00000509536.1:p.His85=
ENST00000688597.1:c.255C>T ENSP00000510628.1:p.His85=
ENST00000690210.1:c.255C>T ENSP00000509272.1:p.His85=
ENST00000692624.1:c.255C>T ENSP00000508953.1:p.His85=
ENST00000351677.7:c.255C>T MANE Select ENSP00000340944.3:p.His85=
ENST00000639857.1:c.255C>T ENSP00000491593.1:p.His85=
ENST00000351677.6:c.255C>T ENSP00000340944.2:p.His85=
ENST00000392597.5:c.255C>T ENSP00000376376.1:p.His85=
ENST00000635625.1:c.255C>T ENSP00000489597.1:p.His85=
NM_002834.3:c.255C>T , LRG_614t1:c.255C>T NP_002825.3:p.His85=
NM_080601.1:c.255C>T NP_542168.1:p.His85=
XM_006719526.1:c.255C>T XP_006719589.1:p.His85=
XM_006719527.1:c.255C>T XP_006719590.1:p.His85=
XM_011538613.1:c.252C>T XP_011536915.1:p.His84=
NM_001330437.1:c.255C>T NP_001317366.1:p.His85=
NM_002834.4:c.255C>T NP_002825.3:p.His85=
NM_080601.2:c.255C>T NP_542168.1:p.His85=
XM_011538613.2:c.252C>T XP_011536915.1:p.His84=
XM_017019722.1:c.252C>T XP_016875211.1:p.His84=
NM_001330437.2:c.255C>T NP_001317366.1:p.His85=
NM_001374625.1:c.252C>T NP_001361554.1:p.His84=
NM_002834.5:c.255C>T MANE Select NP_002825.3:p.His85=
NM_080601.3:c.255C>T NP_542168.1:p.His85=