Canonical Allele Identifier: CA1614757849
Gene: CDKAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.20728455G= , CM000668.2:g.20728455G= GRCh38
NC_000006.11:g.20728686G= , CM000668.1:g.20728686G= GRCh37
NC_000006.10:g.20836665G= NCBI36
NG_021195.1:g.198999G=
NG_021195.2:g.198999G=

Transcript Alleles

HGVS Amino-acid change
ENST00000274695.8:c.372-11064G= MANE Select ENSP00000274695.4:n.372-11064G=
ENST00000378610.1:c.372-11064G= ENSP00000367873.1:n.372-11064G=
NM_017774.3:c.372-11064G= MANE Select NP_060244.2:n.372-11064G=
XM_006715128.2:c.372-11064G= XP_006715191.1:n.372-11064G=
XM_011514718.1:c.372-11064G= XP_011513020.1:n.372-11064G=
XM_011514719.1:c.372-11064G= XP_011513021.1:n.372-11064G=
XR_926265.1:n.539-11064G=
XR_926266.1:n.652-11064G=
XR_926267.1:n.539-11064G=
XM_011514719.2:c.372-11064G= XP_011513021.1:n.372-11064G=
XM_017010986.1:c.372-11064G= XP_016866475.1:n.372-11064G=
XM_017010987.1:c.-383-11064G= XP_016866476.1:n.-383-11064G=
XM_024446481.1:c.372-11064G= XP_024302249.1:n.372-11064G=
XR_001743495.2:n.544-11064G=
XR_001743496.2:n.939-11064G=
XR_001743500.1:n.539-11064G=
XR_001743501.1:n.539-11064G=
XR_926265.2:n.539-11064G=
XR_926266.2:n.652-11064G=
XR_926267.2:n.539-11064G=