Canonical Allele Identifier: CA1086651180
Gene: CDKAL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.20678105_20678106insTTT , CM000668.2:g.20678105_20678106insTTT GRCh38
NC_000006.11:g.20678336_20678337insTTT , CM000668.1:g.20678336_20678337insTTT GRCh37
NC_000006.10:g.20786315_20786316insTTT NCBI36
NG_021195.1:g.148649_148650insTTT
NG_021195.2:g.148649_148650insTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000274695.8:c.371+28728_371+28729insTTT MANE Select ENSP00000274695.4:n.371+28728_371+28729insTTT
ENST00000378610.1:c.371+28728_371+28729insTTT ENSP00000367873.1:n.371+28728_371+28729insTTT
NM_017774.3:c.371+28728_371+28729insTTT MANE Select NP_060244.2:n.371+28728_371+28729insTTT
XM_006715128.2:c.371+28728_371+28729insTTT XP_006715191.1:n.371+28728_371+28729insTTT
XM_011514718.1:c.371+28728_371+28729insTTT XP_011513020.1:n.371+28728_371+28729insTTT
XM_011514719.1:c.371+28728_371+28729insTTT XP_011513021.1:n.371+28728_371+28729insTTT
XR_926265.1:n.538+28728_538+28729insTTT
XR_926266.1:n.651+28728_651+28729insTTT
XR_926267.1:n.538+28728_538+28729insTTT
XM_011514719.2:c.371+28728_371+28729insTTT XP_011513021.1:n.371+28728_371+28729insTTT
XM_017010986.1:c.371+28728_371+28729insTTT XP_016866475.1:n.371+28728_371+28729insTTT
XM_017010987.1:c.-384+28728_-384+28729insTTT XP_016866476.1:n.-384+28728_-384+28729insTTT
XM_024446481.1:c.371+28728_371+28729insTTT XP_024302249.1:n.371+28728_371+28729insTTT
XR_001743495.2:n.543+28728_543+28729insTTT
XR_001743496.2:n.938+28728_938+28729insTTT
XR_001743500.1:n.538+28728_538+28729insTTT
XR_001743501.1:n.538+28728_538+28729insTTT
XR_926265.2:n.538+28728_538+28729insTTT
XR_926266.2:n.651+28728_651+28729insTTT
XR_926267.2:n.538+28728_538+28729insTTT