Canonical Allele Identifier: CA1614664834

Gene: CDKAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.20546466G= , CM000668.2:g.20546466G=	GRCh38
NC_000006.11:g.20546697G= , CM000668.1:g.20546697G=	GRCh37
NC_000006.10:g.20654676G=	NCBI36
NG_021195.1:g.17010G=
NG_021195.2:g.17010G=

Transcript Alleles

HGVS	Amino-acid Change
NM_017774.3:c.116G= MANE Select	NP_060244.2:p.Arg39=
ENST00000274695.8:c.116G= MANE Select	ENSP00000274695.4:p.Arg39=
ENST00000378610.1:c.116G=	ENSP00000367873.1:p.Arg39=
ENST00000613575.4:c.116G=	ENSP00000481755.1:p.Arg39=
XM_006715128.2:c.116G=	XP_006715191.1:p.Arg39=
XM_011514718.1:c.116G=	XP_011513020.1:p.Arg39=
XM_011514719.1:c.116G=	XP_011513021.1:p.Arg39=
XM_011514719.2:c.116G=	XP_011513021.1:p.Arg39=
XM_017010986.1:c.116G=	XP_016866475.1:p.Arg39=
XM_017010987.1:c.-639G=	XP_016866476.1:n.-639G=
XM_024446481.1:c.116G=	XP_024302249.1:p.Arg39=
XR_001743495.2:n.288G=
XR_001743496.2:n.683G=
XR_001743500.1:n.283G=
XR_001743501.1:n.283G=
XR_926265.1:n.283G=
XR_926265.2:n.283G=
XR_926266.1:n.396G=
XR_926266.2:n.396G=
XR_926267.1:n.283G=
XR_926267.2:n.283G=