Canonical Allele Identifier: CA1614687793
Gene: CDKAL1 HGNC NCBI

Linked Data

dbSNP Id: rs1768816624

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.20652445_20652446del , CM000668.2:g.20652445_20652446del GRCh38
NC_000006.11:g.20652676_20652677del , CM000668.1:g.20652676_20652677del GRCh37
NC_000006.10:g.20760655_20760656del NCBI36
NG_021195.1:g.122989_122990del
NG_021195.2:g.122989_122990del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274695.8:c.371+3068_371+3069del MANE Select ENSP00000274695.4:n.371+3068_371+3069del
ENST00000378610.1:c.371+3068_371+3069del ENSP00000367873.1:n.371+3068_371+3069del
NM_017774.3:c.371+3068_371+3069del MANE Select NP_060244.2:n.371+3068_371+3069del
XM_006715128.2:c.371+3068_371+3069del XP_006715191.1:n.371+3068_371+3069del
XM_011514718.1:c.371+3068_371+3069del XP_011513020.1:n.371+3068_371+3069del
XM_011514719.1:c.371+3068_371+3069del XP_011513021.1:n.371+3068_371+3069del
XR_926265.1:n.538+3068_538+3069del
XR_926266.1:n.651+3068_651+3069del
XR_926267.1:n.538+3068_538+3069del
XM_011514719.2:c.371+3068_371+3069del XP_011513021.1:n.371+3068_371+3069del
XM_017010986.1:c.371+3068_371+3069del XP_016866475.1:n.371+3068_371+3069del
XM_017010987.1:c.-384+3068_-384+3069del XP_016866476.1:n.-384+3068_-384+3069del
XM_024446481.1:c.371+3068_371+3069del XP_024302249.1:n.371+3068_371+3069del
XR_001743495.2:n.543+3068_543+3069del
XR_001743496.2:n.938+3068_938+3069del
XR_001743500.1:n.538+3068_538+3069del
XR_001743501.1:n.538+3068_538+3069del
XR_926265.2:n.538+3068_538+3069del
XR_926266.2:n.651+3068_651+3069del
XR_926267.2:n.538+3068_538+3069del