Canonical Allele Identifier: CA951960960
Gene: PTPN11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.112502059C>T , CM000674.2:g.112502059C>T GRCh38
NC_000012.11:g.112939863C>T , CM000674.1:g.112939863C>T GRCh37
NC_000012.10:g.111424246C>T NCBI36
NG_007459.1:g.88328C>T , LRG_614:g.88328C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000639857.2:c.1600-85C>T ENSP00000491593.2:n.1600-85C>T
ENST00000685487.1:c.*802-85C>T ENSP00000508503.1:n.*802-85C>T
ENST00000687120.1:n.898C>T
ENST00000687906.1:c.1486-85C>T ENSP00000509536.1:n.1486-85C>T
ENST00000688597.1:c.1225-85C>T ENSP00000510628.1:n.1225-85C>T
ENST00000688701.1:n.844-85C>T
ENST00000690210.1:c.1600-85C>T ENSP00000509272.1:n.1600-85C>T
ENST00000690472.1:n.809-85C>T
ENST00000692624.1:c.*146-85C>T ENSP00000508953.1:n.*146-85C>T
ENST00000351677.7:c.1600-85C>T MANE Select ENSP00000340944.3:n.1600-85C>T
ENST00000351677.6:c.1600-85C>T ENSP00000340944.2:n.1600-85C>T
ENST00000635625.1:c.1612-85C>T ENSP00000489597.1:n.1612-85C>T
NM_002834.3:c.1600-85C>T , LRG_614t1:c.1600-85C>T NP_002825.3:n.1600-85C>T
XM_006719526.1:c.1612-85C>T XP_006719589.1:n.1612-85C>T
XM_006719527.1:c.1498-85C>T XP_006719590.1:n.1498-85C>T
XM_011538613.1:c.1609-85C>T XP_011536915.1:n.1609-85C>T
NM_001330437.1:c.1612-85C>T NP_001317366.1:n.1612-85C>T
NM_002834.4:c.1600-85C>T NP_002825.3:n.1600-85C>T
XM_011538613.2:c.1609-85C>T XP_011536915.1:n.1609-85C>T
XM_017019722.1:c.1597-85C>T XP_016875211.1:n.1597-85C>T
NM_001330437.2:c.1612-85C>T NP_001317366.1:n.1612-85C>T
NM_001374625.1:c.1597-85C>T NP_001361554.1:n.1597-85C>T
NM_002834.5:c.1600-85C>T MANE Select NP_002825.3:n.1600-85C>T