Canonical Allele Identifier: CA2002773950

Gene: SIK3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116861796G>A , CM000673.2:g.116861796G>A	GRCh38
NC_000011.9:g.116732512G>A , CM000673.1:g.116732512G>A	GRCh37
NC_000011.8:g.116237722G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445177.6:c.2315+45C>T MANE Select	ENSP00000391295.2:n.2315+45C>T
ENST00000375300.6:c.2171+45C>T	ENSP00000364449.1:n.2171+45C>T
ENST00000375300.5:c.2171+45C>T	ENSP00000364449.1:n.2171+45C>T
ENST00000415541.5:c.2151+45C>T	ENSP00000392761.1:n.2151+45C>T
ENST00000445177.5:c.2295+45C>T
ENST00000446921.6:c.2171+45C>T	ENSP00000390442.2:n.2171+45C>T
ENST00000465421.5:n.1613+45C>T
ENST00000488337.5:n.474+45C>T
NM_001281748.1:c.1694+45C>T	NP_001268677.1:n.1694+45C>T
NM_001281749.1:c.2171+45C>T	NP_001268678.1:n.2171+45C>T
NM_025164.4:c.2171+45C>T	NP_079440.3:n.2171+45C>T
XM_005271481.2:c.2315+45C>T	XP_005271538.1:n.2315+45C>T
XM_005271482.3:c.2171+45C>T	XP_005271539.2:n.2171+45C>T
XM_005271484.3:c.2171+45C>T	XP_005271541.2:n.2171+45C>T
XM_005271485.2:c.518+45C>T	XP_005271542.1:n.518+45C>T
XM_005271486.1:c.374+45C>T	XP_005271543.1:n.374+45C>T
XM_011542721.1:c.2315+45C>T	XP_011541023.1:n.2315+45C>T
XM_011542722.1:c.2315+45C>T	XP_011541024.1:n.2315+45C>T
XM_011542723.1:c.1838+45C>T	XP_011541025.1:n.1838+45C>T
XM_011542724.1:c.1838+45C>T	XP_011541026.1:n.1838+45C>T
XM_011542725.1:c.1838+45C>T	XP_011541027.1:n.1838+45C>T
NM_001281748.2:c.1694+45C>T	NP_001268677.1:n.1694+45C>T
NM_001281749.2:c.2171+45C>T	NP_001268678.1:n.2171+45C>T
NM_001366686.1:c.2315+45C>T	NP_001353615.1:n.2315+45C>T
NM_025164.5:c.2171+45C>T	NP_079440.3:n.2171+45C>T
XM_005271482.4:c.2171+45C>T	XP_005271539.2:n.2171+45C>T
XM_005271485.3:c.518+45C>T	XP_005271542.1:n.518+45C>T
XM_011542723.2:c.1838+45C>T	XP_011541025.1:n.1838+45C>T
XM_011542724.2:c.1838+45C>T	XP_011541026.1:n.1838+45C>T
XM_011542725.2:c.1838+45C>T	XP_011541027.1:n.1838+45C>T
XM_017017424.1:c.2027+45C>T	XP_016872913.1:n.2027+45C>T
XM_017017425.1:c.1838+45C>T	XP_016872914.1:n.1838+45C>T
XM_017017426.1:c.1838+45C>T	XP_016872915.1:n.1838+45C>T
XM_017017427.1:c.374+45C>T	XP_016872916.1:n.374+45C>T
NM_001281748.3:c.1694+45C>T	NP_001268677.1:n.1694+45C>T
NM_001281749.3:c.2171+45C>T	NP_001268678.1:n.2171+45C>T
NM_001366686.2:c.2315+45C>T	NP_001353615.1:n.2315+45C>T
NM_025164.6:c.2171+45C>T	NP_079440.3:n.2171+45C>T
NM_001366686.3:c.2315+45C>T MANE Select	NP_001353615.1:n.2315+45C>T