Canonical Allele Identifier: CA135705631
Gene: CDKAL1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs9348440

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.20641105C>T , CM000668.2:g.20641105C>T GRCh38
NC_000006.11:g.20641336C>T , CM000668.1:g.20641336C>T GRCh37
NC_000006.10:g.20749315C>T NCBI36
NG_021195.1:g.111649C>T
NG_021195.2:g.111649C>T

Transcript Alleles

HGVS Amino-acid change
NM_017774.3:c.287-8188C>T VV MANE Preferred NP_060244.2:p.=
XM_006715128.2:c.287-8188C>T XP_006715191.1:p.=
XM_011514718.1:c.287-8188C>T XP_011513020.1:p.=
XM_011514719.1:c.287-8188C>T XP_011513021.1:p.=
XR_926265.1:n.454-8188C>T
XR_926266.1:n.567-8188C>T
XR_926267.1:n.454-8188C>T
XM_011514719.2:c.287-8188C>T XP_011513021.1:p.=
XM_017010986.1:c.287-8188C>T XP_016866475.1:p.=
XM_017010987.1:c.-468-8188C>T XP_016866476.1:p.=
XM_024446481.1:c.287-8188C>T XP_024302249.1:p.=
XR_001743495.2:n.459-8188C>T
XR_001743496.2:n.854-8188C>T
XR_001743500.1:n.454-8188C>T
XR_001743501.1:n.454-8188C>T
XR_926265.2:n.454-8188C>T
XR_926266.2:n.567-8188C>T
XR_926267.2:n.454-8188C>T
ENST00000274695.8:c.287-8188C>T ENSP00000274695.4:p.=
ENST00000378610.1:c.287-8188C>T ENSP00000367873.1:p.=