Canonical Allele Identifier: CA1614758100
Gene: CDKAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.20728566T= , CM000668.2:g.20728566T= GRCh38
NC_000006.11:g.20728797T= , CM000668.1:g.20728797T= GRCh37
NC_000006.10:g.20836776T= NCBI36
NG_021195.1:g.199110T=
NG_021195.2:g.199110T=

Transcript Alleles

HGVS Amino-acid change
ENST00000274695.8:c.372-10953T= MANE Select ENSP00000274695.4:n.372-10953T=
ENST00000378610.1:c.372-10953T= ENSP00000367873.1:n.372-10953T=
NM_017774.3:c.372-10953T= MANE Select NP_060244.2:n.372-10953T=
XM_006715128.2:c.372-10953T= XP_006715191.1:n.372-10953T=
XM_011514718.1:c.372-10953T= XP_011513020.1:n.372-10953T=
XM_011514719.1:c.372-10953T= XP_011513021.1:n.372-10953T=
XR_926265.1:n.539-10953T=
XR_926266.1:n.652-10953T=
XR_926267.1:n.539-10953T=
XM_011514719.2:c.372-10953T= XP_011513021.1:n.372-10953T=
XM_017010986.1:c.372-10953T= XP_016866475.1:n.372-10953T=
XM_017010987.1:c.-383-10953T= XP_016866476.1:n.-383-10953T=
XM_024446481.1:c.372-10953T= XP_024302249.1:n.372-10953T=
XR_001743495.2:n.544-10953T=
XR_001743496.2:n.939-10953T=
XR_001743500.1:n.539-10953T=
XR_001743501.1:n.539-10953T=
XR_926265.2:n.539-10953T=
XR_926266.2:n.652-10953T=
XR_926267.2:n.539-10953T=