Canonical Allele Identifier: CA1139666890
Gene: SIK1 HGNC NCBI

Linked Data

ClinVar Variation Id: 940280
ClinVar RCV Id: RCV001209832
dbSNP Id: rs2081035616

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43417086_43417098del , CM000683.2:g.43417086_43417098del GRCh38
NG_052009.1:g.15043_15055del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270162.8:c.2004_2016del MANE Select ENSP00000270162.6:p.Ala670ProfsTer12
ENST00000270162.6:c.2004_2016del ENSP00000270162.6:p.Ala670ProfsTer12
NM_173354.3:c.2004_2016del NP_775490.2:p.Ala670ProfsTer12
XM_011529474.1:c.1857_1869del XP_011527776.1:p.Ala621ProfsTer12
NM_173354.4:c.2004_2016del NP_775490.2:p.Ala670ProfsTer12
XM_011529474.2:c.1857_1869del XP_011527776.1:p.Ala621ProfsTer12
NM_173354.5:c.2004_2016del MANE Select NP_775490.2:p.Ala670ProfsTer12