Canonical Allele Identifier: CA2002781279

Gene: SIK3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116870893_116870898delinsAAAGAG , CM000673.2:g.116870893_116870898delinsAAAGAG	GRCh38
NC_000011.9:g.116741609_116741614delinsAAAGAG , CM000673.1:g.116741609_116741614delinsAAAGAG	GRCh37
NC_000011.8:g.116246819_116246824delinsAAAGAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445177.6:c.1738-497_1738-492delinsCTCTTT MANE Select	ENSP00000391295.2:n.1738-497_1738-492delinsCTCTTT
ENST00000375300.6:c.1738-497_1738-492delinsCTCTTT	ENSP00000364449.1:n.1738-497_1738-492delinsCTCTTT
ENST00000375300.5:c.1738-497_1738-492delinsCTCTTT	ENSP00000364449.1:n.1738-497_1738-492delinsCTCTTT
ENST00000413553.1:c.1445-497_1445-492delinsCTCTTT
ENST00000415541.5:c.1718-497_1718-492delinsCTCTTT	ENSP00000392761.1:n.1718-497_1718-492delinsCTCTTT
ENST00000445177.5:c.1718-497_1718-492delinsCTCTTT
ENST00000446921.6:c.1594-497_1594-492delinsCTCTTT	ENSP00000390442.2:n.1594-497_1594-492delinsCTCTTT
ENST00000480222.1:n.193-497_193-492delinsCTCTTT
NM_001281748.1:c.1261-497_1261-492delinsCTCTTT	NP_001268677.1:n.1261-497_1261-492delinsCTCTTT
NM_001281749.1:c.1594-497_1594-492delinsCTCTTT	NP_001268678.1:n.1594-497_1594-492delinsCTCTTT
NM_025164.4:c.1738-497_1738-492delinsCTCTTT	NP_079440.3:n.1738-497_1738-492delinsCTCTTT
XM_005271481.2:c.1738-497_1738-492delinsCTCTTT	XP_005271538.1:n.1738-497_1738-492delinsCTCTTT
XM_005271482.3:c.1594-497_1594-492delinsCTCTTT	XP_005271539.2:n.1594-497_1594-492delinsCTCTTT
XM_005271484.3:c.1738-497_1738-492delinsCTCTTT	XP_005271541.2:n.1738-497_1738-492delinsCTCTTT
XM_011542721.1:c.1738-497_1738-492delinsCTCTTT	XP_011541023.1:n.1738-497_1738-492delinsCTCTTT
XM_011542722.1:c.1738-497_1738-492delinsCTCTTT	XP_011541024.1:n.1738-497_1738-492delinsCTCTTT
XM_011542723.1:c.1261-497_1261-492delinsCTCTTT	XP_011541025.1:n.1261-497_1261-492delinsCTCTTT
XM_011542724.1:c.1261-497_1261-492delinsCTCTTT	XP_011541026.1:n.1261-497_1261-492delinsCTCTTT
XM_011542725.1:c.1261-497_1261-492delinsCTCTTT	XP_011541027.1:n.1261-497_1261-492delinsCTCTTT
XM_011542726.1:c.1738-497_1738-492delinsCTCTTT	XP_011541028.1:n.1738-497_1738-492delinsCTCTTT
NM_001281748.2:c.1261-497_1261-492delinsCTCTTT	NP_001268677.1:n.1261-497_1261-492delinsCTCTTT
NM_001281749.2:c.1594-497_1594-492delinsCTCTTT	NP_001268678.1:n.1594-497_1594-492delinsCTCTTT
NM_001366686.1:c.1738-497_1738-492delinsCTCTTT	NP_001353615.1:n.1738-497_1738-492delinsCTCTTT
NM_025164.5:c.1738-497_1738-492delinsCTCTTT	NP_079440.3:n.1738-497_1738-492delinsCTCTTT
XM_005271482.4:c.1594-497_1594-492delinsCTCTTT	XP_005271539.2:n.1594-497_1594-492delinsCTCTTT
XM_011542723.2:c.1261-497_1261-492delinsCTCTTT	XP_011541025.1:n.1261-497_1261-492delinsCTCTTT
XM_011542724.2:c.1261-497_1261-492delinsCTCTTT	XP_011541026.1:n.1261-497_1261-492delinsCTCTTT
XM_011542725.2:c.1261-497_1261-492delinsCTCTTT	XP_011541027.1:n.1261-497_1261-492delinsCTCTTT
XM_017017424.1:c.1594-497_1594-492delinsCTCTTT	XP_016872913.1:n.1594-497_1594-492delinsCTCTTT
XM_017017425.1:c.1261-497_1261-492delinsCTCTTT	XP_016872914.1:n.1261-497_1261-492delinsCTCTTT
XM_017017426.1:c.1261-497_1261-492delinsCTCTTT	XP_016872915.1:n.1261-497_1261-492delinsCTCTTT
XM_017017427.1:c.-250-497_-250-492delinsCTCTTT	XP_016872916.1:n.-250-497_-250-492delinsCTCTTT
XR_001747816.1:n.1776-497_1776-492delinsCTCTTT
NM_001281748.3:c.1261-497_1261-492delinsCTCTTT	NP_001268677.1:n.1261-497_1261-492delinsCTCTTT
NM_001281749.3:c.1594-497_1594-492delinsCTCTTT	NP_001268678.1:n.1594-497_1594-492delinsCTCTTT
NM_001366686.2:c.1738-497_1738-492delinsCTCTTT	NP_001353615.1:n.1738-497_1738-492delinsCTCTTT
NM_025164.6:c.1738-497_1738-492delinsCTCTTT	NP_079440.3:n.1738-497_1738-492delinsCTCTTT
NM_001366686.3:c.1738-497_1738-492delinsCTCTTT MANE Select	NP_001353615.1:n.1738-497_1738-492delinsCTCTTT