Canonical Allele Identifier: CA15477774
Gene: CDKAL1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs9465871

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.20717024T>C , CM000668.2:g.20717024T>C GRCh38
NC_000006.11:g.20717255T>C , CM000668.1:g.20717255T>C GRCh37
NC_000006.10:g.20825234T>C NCBI36
NG_021195.1:g.187568T>C
NG_021195.2:g.187568T>C

Transcript Alleles

HGVS Amino-acid change
NM_017774.3:c.372-22495T>C VV MANE Preferred NP_060244.2:p.=
XM_006715128.2:c.372-22495T>C XP_006715191.1:p.=
XM_011514718.1:c.372-22495T>C XP_011513020.1:p.=
XM_011514719.1:c.372-22495T>C XP_011513021.1:p.=
XR_926265.1:n.539-22495T>C
XR_926266.1:n.652-22495T>C
XR_926267.1:n.539-22495T>C
XM_011514719.2:c.372-22495T>C XP_011513021.1:p.=
XM_017010986.1:c.372-22495T>C XP_016866475.1:p.=
XM_017010987.1:c.-383-22495T>C XP_016866476.1:p.=
XM_024446481.1:c.372-22495T>C XP_024302249.1:p.=
XR_001743495.2:n.544-22495T>C
XR_001743496.2:n.939-22495T>C
XR_001743500.1:n.539-22495T>C
XR_001743501.1:n.539-22495T>C
XR_926265.2:n.539-22495T>C
XR_926266.2:n.652-22495T>C
XR_926267.2:n.539-22495T>C
ENST00000274695.8:c.372-22495T>C ENSP00000274695.4:p.=
ENST00000378610.1:c.372-22495T>C ENSP00000367873.1:p.=