Canonical Allele Identifier: CA1614701735
Gene: CDKAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.20661013_20661014delinsTG , CM000668.2:g.20661013_20661014delinsTG GRCh38
NC_000006.11:g.20661244_20661245delinsTG , CM000668.1:g.20661244_20661245delinsTG GRCh37
NC_000006.10:g.20769223_20769224delinsTG NCBI36
NG_021195.1:g.131557_131558delinsTG
NG_021195.2:g.131557_131558delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000274695.8:c.371+11636_371+11637delinsTG MANE Select ENSP00000274695.4:n.371+11636_371+11637delinsTG
ENST00000378610.1:c.371+11636_371+11637delinsTG ENSP00000367873.1:n.371+11636_371+11637delinsTG
NM_017774.3:c.371+11636_371+11637delinsTG MANE Select NP_060244.2:n.371+11636_371+11637delinsTG
XM_006715128.2:c.371+11636_371+11637delinsTG XP_006715191.1:n.371+11636_371+11637delinsTG
XM_011514718.1:c.371+11636_371+11637delinsTG XP_011513020.1:n.371+11636_371+11637delinsTG
XM_011514719.1:c.371+11636_371+11637delinsTG XP_011513021.1:n.371+11636_371+11637delinsTG
XR_926265.1:n.538+11636_538+11637delinsTG
XR_926266.1:n.651+11636_651+11637delinsTG
XR_926267.1:n.538+11636_538+11637delinsTG
XM_011514719.2:c.371+11636_371+11637delinsTG XP_011513021.1:n.371+11636_371+11637delinsTG
XM_017010986.1:c.371+11636_371+11637delinsTG XP_016866475.1:n.371+11636_371+11637delinsTG
XM_017010987.1:c.-384+11636_-384+11637delinsTG XP_016866476.1:n.-384+11636_-384+11637delinsTG
XM_024446481.1:c.371+11636_371+11637delinsTG XP_024302249.1:n.371+11636_371+11637delinsTG
XR_001743495.2:n.543+11636_543+11637delinsTG
XR_001743496.2:n.938+11636_938+11637delinsTG
XR_001743500.1:n.538+11636_538+11637delinsTG
XR_001743501.1:n.538+11636_538+11637delinsTG
XR_926265.2:n.538+11636_538+11637delinsTG
XR_926266.2:n.651+11636_651+11637delinsTG
XR_926267.2:n.538+11636_538+11637delinsTG