Canonical Allele Identifier: CA1614752999

Gene: CDKAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.20766395G= , CM000668.2:g.20766395G=	GRCh38
NC_000006.11:g.20766626G= , CM000668.1:g.20766626G=	GRCh37
NC_000006.10:g.20874605G=	NCBI36
NG_021195.1:g.236939G=
NG_021195.2:g.236939G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000274695.8:c.517+7752G= MANE Select	ENSP00000274695.4:n.517+7752G=
ENST00000378610.1:c.517+7752G=	ENSP00000367873.1:n.517+7752G=
NM_017774.3:c.517+7752G= MANE Select	NP_060244.2:n.517+7752G=
XM_006715128.2:c.517+7752G=	XP_006715191.1:n.517+7752G=
XM_011514718.1:c.517+7752G=	XP_011513020.1:n.517+7752G=
XM_011514719.1:c.517+7752G=	XP_011513021.1:n.517+7752G=
XR_926265.1:n.684+7752G=
XR_926266.1:n.797+7752G=
XR_926267.1:n.684+7752G=
XM_011514719.2:c.517+7752G=	XP_011513021.1:n.517+7752G=
XM_017010986.1:c.517+7752G=	XP_016866475.1:n.517+7752G=
XM_017010987.1:c.-238+7752G=	XP_016866476.1:n.-238+7752G=
XM_024446481.1:c.517+7752G=	XP_024302249.1:n.517+7752G=
XR_001743495.2:n.689+7752G=
XR_001743496.2:n.1084+7752G=
XR_001743500.1:n.684+7752G=
XR_001743501.1:n.684+7752G=
XR_926265.2:n.684+7752G=
XR_926266.2:n.797+7752G=
XR_926267.2:n.684+7752G=