Canonical Allele Identifier: CA1139662887
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 981578
ClinVar RCV Id: RCV001261098

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.112450355_112450366dup , CM000674.2:g.112450355_112450366dup GRCh38
NC_000012.11:g.112888159_112888170dup , CM000674.1:g.112888159_112888170dup GRCh37
NC_000012.10:g.111372542_111372553dup NCBI36
NG_007459.1:g.36624_36635dup , LRG_614:g.36624_36635dup

Transcript Alleles

HGVS Amino-acid change
ENST00000639857.2:c.175_186dup ENSP00000491593.2:p.Tyr62_Tyr63insThrGlyA...
ENST00000685487.1:c.175_186dup ENSP00000508503.1:p.Tyr62_Tyr63insThrGlyA...
ENST00000687906.1:c.175_186dup ENSP00000509536.1:p.Tyr62_Tyr63insThrGlyA...
ENST00000688597.1:c.175_186dup ENSP00000510628.1:p.Tyr62_Tyr63insThrGlyA...
ENST00000690210.1:c.175_186dup ENSP00000509272.1:p.Tyr62_Tyr63insThrGlyA...
ENST00000692624.1:c.175_186dup ENSP00000508953.1:p.Tyr62_Tyr63insThrGlyA...
ENST00000351677.7:c.175_186dup MANE Select ENSP00000340944.3:p.Tyr62_Tyr63insThrGlyA...
ENST00000639857.1:c.175_186dup ENSP00000491593.1:p.Tyr62_Tyr63insThrGlyA...
ENST00000351677.6:c.175_186dup ENSP00000340944.2:p.Tyr62_Tyr63insThrGlyA...
ENST00000392597.5:c.175_186dup ENSP00000376376.1:p.Tyr62_Tyr63insThrGlyA...
ENST00000635625.1:c.175_186dup ENSP00000489597.1:p.Tyr62_Tyr63insThrGlyA...
NM_002834.3:c.175_186dup , LRG_614t1:c.175_186dup NP_002825.3:p.Tyr62_Tyr63insThrGlyAspTyr
NM_080601.1:c.175_186dup NP_542168.1:p.Tyr62_Tyr63insThrGlyAspTyr
XM_006719526.1:c.175_186dup XP_006719589.1:p.Tyr62_Tyr63insThrGlyAspT...
XM_006719527.1:c.175_186dup XP_006719590.1:p.Tyr62_Tyr63insThrGlyAspT...
XM_011538613.1:c.172_183dup XP_011536915.1:p.Tyr61_Tyr62insThrGlyAspT...
NM_001330437.1:c.175_186dup NP_001317366.1:p.Tyr62_Tyr63insThrGlyAspT...
NM_002834.4:c.175_186dup NP_002825.3:p.Tyr62_Tyr63insThrGlyAspTyr
NM_080601.2:c.175_186dup NP_542168.1:p.Tyr62_Tyr63insThrGlyAspTyr
XM_011538613.2:c.172_183dup XP_011536915.1:p.Tyr61_Tyr62insThrGlyAspT...
XM_017019722.1:c.172_183dup XP_016875211.1:p.Tyr61_Tyr62insThrGlyAspT...
NM_001330437.2:c.175_186dup NP_001317366.1:p.Tyr62_Tyr63insThrGlyAspT...
NM_001374625.1:c.172_183dup NP_001361554.1:p.Tyr61_Tyr62insThrGlyAspT...
NM_002834.5:c.175_186dup MANE Select NP_002825.3:p.Tyr62_Tyr63insThrGlyAspTyr
NM_080601.3:c.175_186dup NP_542168.1:p.Tyr62_Tyr63insThrGlyAspTyr