Canonical Allele Identifier: CA2703497

Gene: TNIK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.171139451T>C , CM000665.2:g.171139451T>C	GRCh38
NC_000003.11:g.170857240T>C , CM000665.1:g.170857240T>C	GRCh37
NC_000003.10:g.172339934T>C	NCBI36
NG_054934.1:g.325958A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_015028.4:c.1419+19A>G MANE Select	NP_055843.1:n.1419+19A>G
ENST00000436636.7:c.1419+19A>G MANE Select	ENSP00000399511.2:n.1419+19A>G
NM_001161560.1:c.1419+19A>G	NP_001155032.1:n.1419+19A>G
NM_001161560.2:c.1419+19A>G	NP_001155032.1:n.1419+19A>G
NM_001161560.3:c.1419+19A>G	NP_001155032.1:n.1419+19A>G
NM_001161561.1:c.1332+948A>G	NP_001155033.1:n.1332+948A>G
NM_001161561.2:c.1332+948A>G	NP_001155033.1:n.1332+948A>G
NM_001161561.3:c.1332+948A>G	NP_001155033.1:n.1332+948A>G
NM_001161562.1:c.1332+948A>G	NP_001155034.1:n.1332+948A>G
NM_001161562.2:c.1332+948A>G	NP_001155034.1:n.1332+948A>G
NM_001161562.3:c.1332+948A>G	NP_001155034.1:n.1332+948A>G
NM_001161563.1:c.1419+19A>G	NP_001155035.1:n.1419+19A>G
NM_001161563.2:c.1419+19A>G	NP_001155035.1:n.1419+19A>G
NM_001161563.3:c.1419+19A>G	NP_001155035.1:n.1419+19A>G
NM_001161564.1:c.1419+19A>G	NP_001155036.1:n.1419+19A>G
NM_001161564.2:c.1419+19A>G	NP_001155036.1:n.1419+19A>G
NM_001161564.3:c.1419+19A>G	NP_001155036.1:n.1419+19A>G
NM_001161565.1:c.1332+948A>G	NP_001155037.1:n.1332+948A>G
NM_001161565.2:c.1332+948A>G	NP_001155037.1:n.1332+948A>G
NM_001161565.3:c.1332+948A>G	NP_001155037.1:n.1332+948A>G
NM_001161566.1:c.1332+948A>G	NP_001155038.1:n.1332+948A>G
NM_001161566.2:c.1332+948A>G	NP_001155038.1:n.1332+948A>G
NM_001161566.3:c.1332+948A>G	NP_001155038.1:n.1332+948A>G
NM_015028.2:c.1419+19A>G	NP_055843.1:n.1419+19A>G
NM_015028.3:c.1419+19A>G	NP_055843.1:n.1419+19A>G
ENST00000284483.12:c.1419+19A>G	ENSP00000284483.8:n.1419+19A>G
ENST00000341852.10:c.1332+948A>G	ENSP00000345352.6:n.1332+948A>G
ENST00000357327.9:c.1332+948A>G	ENSP00000349880.5:n.1332+948A>G
ENST00000436636.6:c.1419+19A>G	ENSP00000399511.2:n.1419+19A>G
ENST00000460047.5:c.1419+19A>G	ENSP00000418916.1:n.1419+19A>G
ENST00000470834.5:c.1332+948A>G	ENSP00000419990.1:n.1332+948A>G
ENST00000475336.5:c.1332+948A>G	ENSP00000418156.1:n.1332+948A>G
ENST00000488470.5:c.1419+19A>G	ENSP00000418378.1:n.1419+19A>G
XR_001740525.1:n.1370-5457T>C
XR_924712.1:n.908-5457T>C