Canonical Allele Identifier: CA2711405982
Gene: CDKAL1 HGNC NCBI

Linked Data

dbSNP Id: rs2127789427

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.20679304_20679305del , CM000668.2:g.20679304_20679305del GRCh38
NC_000006.11:g.20679535_20679536del , CM000668.1:g.20679535_20679536del GRCh37
NC_000006.10:g.20787514_20787515del NCBI36
NG_021195.1:g.149848_149849del
NG_021195.2:g.149848_149849del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274695.8:c.371+29927_371+29928del MANE Select ENSP00000274695.4:n.371+29927_371+29928del
ENST00000378610.1:c.371+29927_371+29928del ENSP00000367873.1:n.371+29927_371+29928del
NM_017774.3:c.371+29927_371+29928del MANE Select NP_060244.2:n.371+29927_371+29928del
XM_006715128.2:c.371+29927_371+29928del XP_006715191.1:n.371+29927_371+29928del
XM_011514718.1:c.371+29927_371+29928del XP_011513020.1:n.371+29927_371+29928del
XM_011514719.1:c.371+29927_371+29928del XP_011513021.1:n.371+29927_371+29928del
XR_926265.1:n.538+29927_538+29928del
XR_926266.1:n.651+29927_651+29928del
XR_926267.1:n.538+29927_538+29928del
XM_011514719.2:c.371+29927_371+29928del XP_011513021.1:n.371+29927_371+29928del
XM_017010986.1:c.371+29927_371+29928del XP_016866475.1:n.371+29927_371+29928del
XM_017010987.1:c.-384+29927_-384+29928del XP_016866476.1:n.-384+29927_-384+29928del
XM_024446481.1:c.371+29927_371+29928del XP_024302249.1:n.371+29927_371+29928del
XR_001743495.2:n.543+29927_543+29928del
XR_001743496.2:n.938+29927_938+29928del
XR_001743500.1:n.538+29927_538+29928del
XR_001743501.1:n.538+29927_538+29928del
XR_926265.2:n.538+29927_538+29928del
XR_926266.2:n.651+29927_651+29928del
XR_926267.2:n.538+29927_538+29928del