Canonical Allele Identifier: CA1614822054
Gene: CDKAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.20856516_20856517delinsAT , CM000668.2:g.20856516_20856517delinsAT GRCh38
NC_000006.11:g.20856747_20856748delinsAT , CM000668.1:g.20856747_20856748delinsAT GRCh37
NC_000006.10:g.20964726_20964727delinsAT NCBI36
NG_021195.1:g.327060_327061delinsAT
NG_021195.2:g.327060_327061delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000274695.8:c.742+10338_742+10339delinsAT MANE Select ENSP00000274695.4:n.742+10338_742+10339delinsAT
ENST00000378610.1:c.742+10338_742+10339delinsAT ENSP00000367873.1:n.742+10338_742+10339delinsAT
NM_017774.3:c.742+10338_742+10339delinsAT MANE Select NP_060244.2:n.742+10338_742+10339delinsAT
XM_006715128.2:c.742+10338_742+10339delinsAT XP_006715191.1:n.742+10338_742+10339delinsAT
XM_011514718.1:c.742+10338_742+10339delinsAT XP_011513020.1:n.742+10338_742+10339delinsAT
XM_011514719.1:c.742+10338_742+10339delinsAT XP_011513021.1:n.742+10338_742+10339delinsAT
XR_926265.1:n.909+10338_909+10339delinsAT
XR_926266.1:n.1022+10338_1022+10339delinsAT
XR_926267.1:n.909+10338_909+10339delinsAT
XM_011514719.2:c.742+10338_742+10339delinsAT XP_011513021.1:n.742+10338_742+10339delinsAT
XM_017010986.1:c.742+10338_742+10339delinsAT XP_016866475.1:n.742+10338_742+10339delinsAT
XM_017010987.1:c.-117+75251_-117+75252delinsAT XP_016866476.1:n.-117+75251_-117+75252delinsAT
XM_024446481.1:c.742+10338_742+10339delinsAT XP_024302249.1:n.742+10338_742+10339delinsAT
XR_001743495.2:n.914+10338_914+10339delinsAT
XR_001743496.2:n.1309+10338_1309+10339delinsAT
XR_001743498.2:n.2641+10338_2641+10339delinsAT
XR_001743500.1:n.909+10338_909+10339delinsAT
XR_001743501.1:n.909+10338_909+10339delinsAT
XR_926265.2:n.909+10338_909+10339delinsAT
XR_926266.2:n.1022+10338_1022+10339delinsAT
XR_926267.2:n.909+10338_909+10339delinsAT