Canonical Allele Identifier: CA229332715
Gene: SIK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116912258T>G , CM000673.2:g.116912258T>G GRCh38
NC_000011.9:g.116782974T>G , CM000673.1:g.116782974T>G GRCh37
NC_000011.8:g.116288184T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000445177.6:c.617-14941A>C MANE Select ENSP00000391295.2:n.617-14941A>C
ENST00000375300.6:c.617-14941A>C ENSP00000364449.1:n.617-14941A>C
ENST00000375300.5:c.617-14941A>C ENSP00000364449.1:n.617-14941A>C
ENST00000413553.1:c.324-14941A>C
ENST00000415541.5:c.597-14941A>C ENSP00000392761.1:n.597-14941A>C
ENST00000445177.5:c.597-14941A>C
ENST00000446921.6:c.617-14941A>C ENSP00000390442.2:n.617-14941A>C
ENST00000485363.1:n.507-7255A>C
ENST00000497049.5:n.344-14941A>C
NM_001281748.1:c.140-14941A>C NP_001268677.1:n.140-14941A>C
NM_001281749.1:c.617-14941A>C NP_001268678.1:n.617-14941A>C
NM_025164.4:c.617-14941A>C NP_079440.3:n.617-14941A>C
XM_005271481.2:c.617-14941A>C XP_005271538.1:n.617-14941A>C
XM_005271482.3:c.617-14941A>C XP_005271539.2:n.617-14941A>C
XM_005271484.3:c.617-14941A>C XP_005271541.2:n.617-14941A>C
XM_011542721.1:c.617-14941A>C XP_011541023.1:n.617-14941A>C
XM_011542722.1:c.617-14941A>C XP_011541024.1:n.617-14941A>C
XM_011542723.1:c.140-14941A>C XP_011541025.1:n.140-14941A>C
XM_011542724.1:c.140-14941A>C XP_011541026.1:n.140-14941A>C
XM_011542725.1:c.140-14941A>C XP_011541027.1:n.140-14941A>C
XM_011542726.1:c.617-14941A>C XP_011541028.1:n.617-14941A>C
NM_001281748.2:c.140-14941A>C NP_001268677.1:n.140-14941A>C
NM_001281749.2:c.617-14941A>C NP_001268678.1:n.617-14941A>C
NM_001366686.1:c.617-14941A>C NP_001353615.1:n.617-14941A>C
NM_001366687.1:c.617-7255A>C NP_001353616.1:n.617-7255A>C
NM_025164.5:c.617-14941A>C NP_079440.3:n.617-14941A>C
XM_005271482.4:c.617-14941A>C XP_005271539.2:n.617-14941A>C
XM_011542723.2:c.140-14941A>C XP_011541025.1:n.140-14941A>C
XM_011542724.2:c.140-14941A>C XP_011541026.1:n.140-14941A>C
XM_011542725.2:c.140-14941A>C XP_011541027.1:n.140-14941A>C
XM_017017424.1:c.617-14941A>C XP_016872913.1:n.617-14941A>C
XM_017017425.1:c.140-14941A>C XP_016872914.1:n.140-14941A>C
XM_017017426.1:c.140-14941A>C XP_016872915.1:n.140-14941A>C
XR_001747816.1:n.655-14941A>C
NM_001281748.3:c.140-14941A>C NP_001268677.1:n.140-14941A>C
NM_001281749.3:c.617-14941A>C NP_001268678.1:n.617-14941A>C
NM_001366686.2:c.617-14941A>C NP_001353615.1:n.617-14941A>C
NM_025164.6:c.617-14941A>C NP_079440.3:n.617-14941A>C
NM_001366686.3:c.617-14941A>C MANE Select NP_001353615.1:n.617-14941A>C