Canonical Allele Identifier: CA1614822223

Gene: CDKAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.20856631T= , CM000668.2:g.20856631T=	GRCh38
NC_000006.11:g.20856862T= , CM000668.1:g.20856862T=	GRCh37
NC_000006.10:g.20964841T=	NCBI36
NG_021195.1:g.327175T=
NG_021195.2:g.327175T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274695.8:c.742+10453T= MANE Select	ENSP00000274695.4:n.742+10453T=
ENST00000378610.1:c.742+10453T=	ENSP00000367873.1:n.742+10453T=
NM_017774.3:c.742+10453T= MANE Select	NP_060244.2:n.742+10453T=
XM_006715128.2:c.742+10453T=	XP_006715191.1:n.742+10453T=
XM_011514718.1:c.742+10453T=	XP_011513020.1:n.742+10453T=
XM_011514719.1:c.742+10453T=	XP_011513021.1:n.742+10453T=
XR_926265.1:n.909+10453T=
XR_926266.1:n.1022+10453T=
XR_926267.1:n.909+10453T=
XM_011514719.2:c.742+10453T=	XP_011513021.1:n.742+10453T=
XM_017010986.1:c.742+10453T=	XP_016866475.1:n.742+10453T=
XM_017010987.1:c.-117+75366T=	XP_016866476.1:n.-117+75366T=
XM_024446481.1:c.742+10453T=	XP_024302249.1:n.742+10453T=
XR_001743495.2:n.914+10453T=
XR_001743496.2:n.1309+10453T=
XR_001743498.2:n.2641+10453T=
XR_001743500.1:n.909+10453T=
XR_001743501.1:n.909+10453T=
XR_926265.2:n.909+10453T=
XR_926266.2:n.1022+10453T=
XR_926267.2:n.909+10453T=