Canonical Allele Identifier: CA915272817
Gene: CDKAL1 HGNC NCBI

Linked Data

dbSNP Id: rs1562020344
gnomAD v2: 6-20679772-C-G
gnomAD v3: 6-20679541-C-G
gnomAD v4: 6-20679541-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.20679541C>G , CM000668.2:g.20679541C>G GRCh38
NC_000006.11:g.20679772C>G , CM000668.1:g.20679772C>G GRCh37
NC_000006.10:g.20787751C>G NCBI36
NG_021195.1:g.150085C>G
NG_021195.2:g.150085C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274695.8:c.371+30164C>G MANE Select ENSP00000274695.4:n.371+30164C>G
ENST00000378610.1:c.371+30164C>G ENSP00000367873.1:n.371+30164C>G
NM_017774.3:c.371+30164C>G MANE Select NP_060244.2:n.371+30164C>G
XM_006715128.2:c.371+30164C>G XP_006715191.1:n.371+30164C>G
XM_011514718.1:c.371+30164C>G XP_011513020.1:n.371+30164C>G
XM_011514719.1:c.371+30164C>G XP_011513021.1:n.371+30164C>G
XR_926265.1:n.538+30164C>G
XR_926266.1:n.651+30164C>G
XR_926267.1:n.538+30164C>G
XM_011514719.2:c.371+30164C>G XP_011513021.1:n.371+30164C>G
XM_017010986.1:c.371+30164C>G XP_016866475.1:n.371+30164C>G
XM_017010987.1:c.-384+30164C>G XP_016866476.1:n.-384+30164C>G
XM_024446481.1:c.371+30164C>G XP_024302249.1:n.371+30164C>G
XR_001743495.2:n.543+30164C>G
XR_001743496.2:n.938+30164C>G
XR_001743500.1:n.538+30164C>G
XR_001743501.1:n.538+30164C>G
XR_926265.2:n.538+30164C>G
XR_926266.2:n.651+30164C>G
XR_926267.2:n.538+30164C>G