Canonical Allele Identifier: CA2703081
Community Standard Title: NM_015028.4(TNIK):c.2869A>G (p.Met957Val)
Gene: TNIK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.171087359T>C , CM000665.2:g.171087359T>C GRCh38
NC_000003.11:g.170805148T>C , CM000665.1:g.170805148T>C GRCh37
NC_000003.10:g.172287842T>C NCBI36
NG_054934.1:g.378050A>G

Transcript Alleles

HGVS Amino-acid Change
NM_015028.4:c.2869A>G MANE Select NP_055843.1:p.Met957Val
ENST00000436636.7:c.2869A>G MANE Select ENSP00000399511.2:p.Met957Val
NM_001161560.1:c.2845A>G NP_001155032.1:p.Met949Val
NM_001161560.2:c.2845A>G NP_001155032.1:p.Met949Val
NM_001161560.3:c.2845A>G NP_001155032.1:p.Met949Val
NM_001161561.1:c.2782A>G NP_001155033.1:p.Met928Val
NM_001161561.2:c.2782A>G NP_001155033.1:p.Met928Val
NM_001161561.3:c.2782A>G NP_001155033.1:p.Met928Val
NM_001161562.1:c.2758A>G NP_001155034.1:p.Met920Val
NM_001161562.2:c.2758A>G NP_001155034.1:p.Met920Val
NM_001161562.3:c.2758A>G NP_001155034.1:p.Met920Val
NM_001161563.1:c.2704A>G NP_001155035.1:p.Met902Val
NM_001161563.2:c.2704A>G NP_001155035.1:p.Met902Val
NM_001161563.3:c.2704A>G NP_001155035.1:p.Met902Val
NM_001161564.1:c.2680A>G NP_001155036.1:p.Met894Val
NM_001161564.2:c.2680A>G NP_001155036.1:p.Met894Val
NM_001161564.3:c.2680A>G NP_001155036.1:p.Met894Val
NM_001161565.1:c.2617A>G NP_001155037.1:p.Met873Val
NM_001161565.2:c.2617A>G NP_001155037.1:p.Met873Val
NM_001161565.3:c.2617A>G NP_001155037.1:p.Met873Val
NM_001161566.1:c.2593A>G NP_001155038.1:p.Met865Val
NM_001161566.2:c.2593A>G NP_001155038.1:p.Met865Val
NM_001161566.3:c.2593A>G NP_001155038.1:p.Met865Val
NM_015028.2:c.2869A>G NP_055843.1:p.Met957Val
NM_015028.3:c.2869A>G NP_055843.1:p.Met957Val
ENST00000284483.12:c.2845A>G ENSP00000284483.8:p.Met949Val
ENST00000341852.10:c.2617A>G ENSP00000345352.6:p.Met873Val
ENST00000357327.9:c.2782A>G ENSP00000349880.5:p.Met928Val
ENST00000436636.6:c.2869A>G ENSP00000399511.2:p.Met957Val
ENST00000460047.5:c.2680A>G ENSP00000418916.1:p.Met894Val
ENST00000470834.5:c.2758A>G ENSP00000419990.1:p.Met920Val
ENST00000475336.5:c.2593A>G ENSP00000418156.1:p.Met865Val
ENST00000488470.5:c.2704A>G ENSP00000418378.1:p.Met902Val
ENST00000496492.5:n.902A>G