Canonical Allele Identifier: CA3858701
Gene: CILK1 HGNC NCBI

Linked Data

ClinVar Variation Id: 593881
ClinVar RCV Id: RCV000729048
dbSNP Id: rs151237769
gnomAD v2: 6-52880927-C-T
gnomAD v3: 6-53016129-C-T
gnomAD v4: 6-53016129-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.53016129C>T , CM000668.2:g.53016129C>T GRCh38
NC_000006.11:g.52880927C>T , CM000668.1:g.52880927C>T GRCh37
NC_000006.10:g.52988886C>T NCBI36
NG_012159.1:g.50674G>A
NG_012159.2:g.50674G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000350082.10:c.785G>A ENSP00000263043.8:p.Arg262Lys
ENST00000676107.1:c.785G>A MANE Select ENSP00000501692.1:p.Arg262Lys
ENST00000350082.9:c.785G>A ENSP00000263043.7:p.Arg262Lys
ENST00000356971.3:c.785G>A ENSP00000349458.3:p.Arg262Lys
NM_014920.3:c.785G>A NP_055735.1:p.Arg262Lys
NM_016513.4:c.785G>A NP_057597.2:p.Arg262Lys
XM_011514419.1:c.785G>A XP_011512721.1:p.Arg262Lys
XM_011514420.1:c.785G>A XP_011512722.1:p.Arg262Lys
XM_011514421.1:c.785G>A XP_011512723.1:p.Arg262Lys
XM_011514420.2:c.785G>A XP_011512722.1:p.Arg262Lys
XM_017010485.1:c.785G>A XP_016865974.1:p.Arg262Lys
XM_017010486.1:c.785G>A XP_016865975.1:p.Arg262Lys
XM_017010487.1:c.785G>A XP_016865976.1:p.Arg262Lys
XM_017010488.1:c.785G>A XP_016865977.1:p.Arg262Lys
XM_017010489.1:c.785G>A XP_016865978.1:p.Arg262Lys
XM_017010490.1:c.785G>A XP_016865979.1:p.Arg262Lys
XM_017010491.1:c.785G>A XP_016865980.1:p.Arg262Lys
XM_017010492.1:c.785G>A XP_016865981.1:p.Arg262Lys
NM_001375397.1:c.785G>A NP_001362326.1:p.Arg262Lys
NM_001375398.1:c.785G>A NP_001362327.1:p.Arg262Lys
NM_001375399.1:c.785G>A NP_001362328.1:p.Arg262Lys
NM_001375400.1:c.785G>A NP_001362329.1:p.Arg262Lys
NM_001375401.1:c.785G>A NP_001362330.1:p.Arg262Lys
NM_001375402.1:c.785G>A NP_001362331.1:p.Arg262Lys
NM_014920.5:c.785G>A MANE Select NP_055735.1:p.Arg262Lys
NM_016513.5:c.785G>A NP_057597.2:p.Arg262Lys
NR_164684.1:n.1186G>A