Canonical Allele Identifier: CA2842080721
Gene: SIK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116870912G>T , CM000673.2:g.116870912G>T GRCh38
NC_000011.9:g.116741628G>T , CM000673.1:g.116741628G>T GRCh37
NC_000011.8:g.116246838G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000445177.6:c.1738-511C>A MANE Select ENSP00000391295.2:n.1738-511C>A
ENST00000375300.6:c.1738-511C>A ENSP00000364449.1:n.1738-511C>A
ENST00000375300.5:c.1738-511C>A ENSP00000364449.1:n.1738-511C>A
ENST00000413553.1:c.1445-511C>A
ENST00000415541.5:c.1718-511C>A ENSP00000392761.1:n.1718-511C>A
ENST00000445177.5:c.1718-511C>A
ENST00000446921.6:c.1594-511C>A ENSP00000390442.2:n.1594-511C>A
ENST00000480222.1:n.193-511C>A
NM_001281748.1:c.1261-511C>A NP_001268677.1:n.1261-511C>A
NM_001281749.1:c.1594-511C>A NP_001268678.1:n.1594-511C>A
NM_025164.4:c.1738-511C>A NP_079440.3:n.1738-511C>A
XM_005271481.2:c.1738-511C>A XP_005271538.1:n.1738-511C>A
XM_005271482.3:c.1594-511C>A XP_005271539.2:n.1594-511C>A
XM_005271484.3:c.1738-511C>A XP_005271541.2:n.1738-511C>A
XM_011542721.1:c.1738-511C>A XP_011541023.1:n.1738-511C>A
XM_011542722.1:c.1738-511C>A XP_011541024.1:n.1738-511C>A
XM_011542723.1:c.1261-511C>A XP_011541025.1:n.1261-511C>A
XM_011542724.1:c.1261-511C>A XP_011541026.1:n.1261-511C>A
XM_011542725.1:c.1261-511C>A XP_011541027.1:n.1261-511C>A
XM_011542726.1:c.1738-511C>A XP_011541028.1:n.1738-511C>A
NM_001281748.2:c.1261-511C>A NP_001268677.1:n.1261-511C>A
NM_001281749.2:c.1594-511C>A NP_001268678.1:n.1594-511C>A
NM_001366686.1:c.1738-511C>A NP_001353615.1:n.1738-511C>A
NM_025164.5:c.1738-511C>A NP_079440.3:n.1738-511C>A
XM_005271482.4:c.1594-511C>A XP_005271539.2:n.1594-511C>A
XM_011542723.2:c.1261-511C>A XP_011541025.1:n.1261-511C>A
XM_011542724.2:c.1261-511C>A XP_011541026.1:n.1261-511C>A
XM_011542725.2:c.1261-511C>A XP_011541027.1:n.1261-511C>A
XM_017017424.1:c.1594-511C>A XP_016872913.1:n.1594-511C>A
XM_017017425.1:c.1261-511C>A XP_016872914.1:n.1261-511C>A
XM_017017426.1:c.1261-511C>A XP_016872915.1:n.1261-511C>A
XM_017017427.1:c.-250-511C>A XP_016872916.1:n.-250-511C>A
XR_001747816.1:n.1776-511C>A
NM_001281748.3:c.1261-511C>A NP_001268677.1:n.1261-511C>A
NM_001281749.3:c.1594-511C>A NP_001268678.1:n.1594-511C>A
NM_001366686.2:c.1738-511C>A NP_001353615.1:n.1738-511C>A
NM_025164.6:c.1738-511C>A NP_079440.3:n.1738-511C>A
NM_001366686.3:c.1738-511C>A MANE Select NP_001353615.1:n.1738-511C>A