Canonical Allele Identifier: CA1614757761

Gene: CDKAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.20728369T= , CM000668.2:g.20728369T=	GRCh38
NC_000006.11:g.20728600T= , CM000668.1:g.20728600T=	GRCh37
NC_000006.10:g.20836579T=	NCBI36
NG_021195.1:g.198913T=
NG_021195.2:g.198913T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274695.8:c.372-11150T= MANE Select	ENSP00000274695.4:n.372-11150T=
ENST00000378610.1:c.372-11150T=	ENSP00000367873.1:n.372-11150T=
NM_017774.3:c.372-11150T= MANE Select	NP_060244.2:n.372-11150T=
XM_006715128.2:c.372-11150T=	XP_006715191.1:n.372-11150T=
XM_011514718.1:c.372-11150T=	XP_011513020.1:n.372-11150T=
XM_011514719.1:c.372-11150T=	XP_011513021.1:n.372-11150T=
XR_926265.1:n.539-11150T=
XR_926266.1:n.652-11150T=
XR_926267.1:n.539-11150T=
XM_011514719.2:c.372-11150T=	XP_011513021.1:n.372-11150T=
XM_017010986.1:c.372-11150T=	XP_016866475.1:n.372-11150T=
XM_017010987.1:c.-383-11150T=	XP_016866476.1:n.-383-11150T=
XM_024446481.1:c.372-11150T=	XP_024302249.1:n.372-11150T=
XR_001743495.2:n.544-11150T=
XR_001743496.2:n.939-11150T=
XR_001743500.1:n.539-11150T=
XR_001743501.1:n.539-11150T=
XR_926265.2:n.539-11150T=
XR_926266.2:n.652-11150T=
XR_926267.2:n.539-11150T=