Canonical Allele Identifier: CA566057694

Gene: CDKAL1

Linked Data

• dbSNP Id: rs1412935392
• gnomAD v2: 6-20728803-TG-T
• gnomAD v3: 6-20728572-TG-T
• gnomAD v4: 6-20728572-TG-T
• MyVariant Identifiers: chr6:g.20728804del (hg19) ; chr6:g.20728573del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.20728573del , CM000668.2:g.20728573del	GRCh38
NC_000006.11:g.20728804del , CM000668.1:g.20728804del	GRCh37
NC_000006.10:g.20836783del	NCBI36
NG_021195.1:g.199117del
NG_021195.2:g.199117del

Transcript Alleles

HGVS	Amino-acid change
ENST00000274695.8:c.372-10946del MANE Select	ENSP00000274695.4:n.372-10946del
ENST00000378610.1:c.372-10946del	ENSP00000367873.1:n.372-10946del
NM_017774.3:c.372-10946del MANE Select	NP_060244.2:n.372-10946del
XM_006715128.2:c.372-10946del	XP_006715191.1:n.372-10946del
XM_011514718.1:c.372-10946del	XP_011513020.1:n.372-10946del
XM_011514719.1:c.372-10946del	XP_011513021.1:n.372-10946del
XR_926265.1:n.539-10946del
XR_926266.1:n.652-10946del
XR_926267.1:n.539-10946del
XM_011514719.2:c.372-10946del	XP_011513021.1:n.372-10946del
XM_017010986.1:c.372-10946del	XP_016866475.1:n.372-10946del
XM_017010987.1:c.-383-10946del	XP_016866476.1:n.-383-10946del
XM_024446481.1:c.372-10946del	XP_024302249.1:n.372-10946del
XR_001743495.2:n.544-10946del
XR_001743496.2:n.939-10946del
XR_001743500.1:n.539-10946del
XR_001743501.1:n.539-10946del
XR_926265.2:n.539-10946del
XR_926266.2:n.652-10946del
XR_926267.2:n.539-10946del