Canonical Allele Identifier: CA1614729735
Gene: CDKAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.20812455C= , CM000668.2:g.20812455C= GRCh38
NC_000006.11:g.20812686C= , CM000668.1:g.20812686C= GRCh37
NC_000006.10:g.20920665C= NCBI36
NG_021195.1:g.282999C=
NG_021195.2:g.282999C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274695.8:c.638+31190C= MANE Select ENSP00000274695.4:n.638+31190C=
ENST00000378610.1:c.638+31190C= ENSP00000367873.1:n.638+31190C=
NM_017774.3:c.638+31190C= MANE Select NP_060244.2:n.638+31190C=
XM_006715128.2:c.638+31190C= XP_006715191.1:n.638+31190C=
XM_011514718.1:c.638+31190C= XP_011513020.1:n.638+31190C=
XM_011514719.1:c.638+31190C= XP_011513021.1:n.638+31190C=
XR_926265.1:n.805+31190C=
XR_926266.1:n.918+31190C=
XR_926267.1:n.805+31190C=
XM_011514719.2:c.638+31190C= XP_011513021.1:n.638+31190C=
XM_017010986.1:c.638+31190C= XP_016866475.1:n.638+31190C=
XM_017010987.1:c.-117+31190C= XP_016866476.1:n.-117+31190C=
XM_024446481.1:c.638+31190C= XP_024302249.1:n.638+31190C=
XR_001743495.2:n.810+31190C=
XR_001743496.2:n.1205+31190C=
XR_001743498.2:n.2537+31190C=
XR_001743500.1:n.805+31190C=
XR_001743501.1:n.805+31190C=
XR_926265.2:n.805+31190C=
XR_926266.2:n.918+31190C=
XR_926267.2:n.805+31190C=