Canonical Allele Identifier: CA566057684
Gene: CDKAL1 HGNC NCBI

Linked Data

dbSNP Id: rs1257437507

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.20728498_20728499insTTTT , CM000668.2:g.20728498_20728499insTTTT GRCh38
NC_000006.11:g.20728729_20728730insTTTT , CM000668.1:g.20728729_20728730insTTTT GRCh37
NC_000006.10:g.20836708_20836709insTTTT NCBI36
NG_021195.1:g.199042_199043insTTTT
NG_021195.2:g.199042_199043insTTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000274695.8:c.372-11021_372-11020insTTTT MANE Select ENSP00000274695.4:n.372-11021_372-11020in...
ENST00000378610.1:c.372-11021_372-11020insTTTT ENSP00000367873.1:n.372-11021_372-11020in...
NM_017774.3:c.372-11021_372-11020insTTTT MANE Select NP_060244.2:n.372-11021_372-11020insTTTT
XM_006715128.2:c.372-11021_372-11020insTTTT XP_006715191.1:n.372-11021_372-11020insTT...
XM_011514718.1:c.372-11021_372-11020insTTTT XP_011513020.1:n.372-11021_372-11020insTT...
XM_011514719.1:c.372-11021_372-11020insTTTT XP_011513021.1:n.372-11021_372-11020insTT...
XR_926265.1:n.539-11021_539-11020insTTTT
XR_926266.1:n.652-11021_652-11020insTTTT
XR_926267.1:n.539-11021_539-11020insTTTT
XM_011514719.2:c.372-11021_372-11020insTTTT XP_011513021.1:n.372-11021_372-11020insTT...
XM_017010986.1:c.372-11021_372-11020insTTTT XP_016866475.1:n.372-11021_372-11020insTT...
XM_017010987.1:c.-383-11021_-383-11020insTTTT XP_016866476.1:n.-383-11021_-383-11020ins...
XM_024446481.1:c.372-11021_372-11020insTTTT XP_024302249.1:n.372-11021_372-11020insTT...
XR_001743495.2:n.544-11021_544-11020insTTTT
XR_001743496.2:n.939-11021_939-11020insTTTT
XR_001743500.1:n.539-11021_539-11020insTTTT
XR_001743501.1:n.539-11021_539-11020insTTTT
XR_926265.2:n.539-11021_539-11020insTTTT
XR_926266.2:n.652-11021_652-11020insTTTT
XR_926267.2:n.539-11021_539-11020insTTTT