Canonical Allele Identifier: CA1614710023
Gene: CDKAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.20640966T= , CM000668.2:g.20640966T= GRCh38
NC_000006.11:g.20641197T= , CM000668.1:g.20641197T= GRCh37
NC_000006.10:g.20749176T= NCBI36
NG_021195.1:g.111510T=
NG_021195.2:g.111510T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274695.8:c.287-8327T= MANE Select ENSP00000274695.4:n.287-8327T=
ENST00000378610.1:c.287-8327T= ENSP00000367873.1:n.287-8327T=
NM_017774.3:c.287-8327T= MANE Select NP_060244.2:n.287-8327T=
XM_006715128.2:c.287-8327T= XP_006715191.1:n.287-8327T=
XM_011514718.1:c.287-8327T= XP_011513020.1:n.287-8327T=
XM_011514719.1:c.287-8327T= XP_011513021.1:n.287-8327T=
XR_926265.1:n.454-8327T=
XR_926266.1:n.567-8327T=
XR_926267.1:n.454-8327T=
XM_011514719.2:c.287-8327T= XP_011513021.1:n.287-8327T=
XM_017010986.1:c.287-8327T= XP_016866475.1:n.287-8327T=
XM_017010987.1:c.-468-8327T= XP_016866476.1:n.-468-8327T=
XM_024446481.1:c.287-8327T= XP_024302249.1:n.287-8327T=
XR_001743495.2:n.459-8327T=
XR_001743496.2:n.854-8327T=
XR_001743500.1:n.454-8327T=
XR_001743501.1:n.454-8327T=
XR_926265.2:n.454-8327T=
XR_926266.2:n.567-8327T=
XR_926267.2:n.454-8327T=