Canonical Allele Identifier: CA2770235708
Gene: CDKAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.20678103_20678104insCTT , CM000668.2:g.20678103_20678104insCTT GRCh38
NC_000006.11:g.20678334_20678335insCTT , CM000668.1:g.20678334_20678335insCTT GRCh37
NC_000006.10:g.20786313_20786314insCTT NCBI36
NG_021195.1:g.148647_148648insCTT
NG_021195.2:g.148647_148648insCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000274695.8:c.371+28726_371+28727insCTT MANE Select ENSP00000274695.4:n.371+28726_371+28727insCTT
ENST00000378610.1:c.371+28726_371+28727insCTT ENSP00000367873.1:n.371+28726_371+28727insCTT
NM_017774.3:c.371+28726_371+28727insCTT MANE Select NP_060244.2:n.371+28726_371+28727insCTT
XM_006715128.2:c.371+28726_371+28727insCTT XP_006715191.1:n.371+28726_371+28727insCTT
XM_011514718.1:c.371+28726_371+28727insCTT XP_011513020.1:n.371+28726_371+28727insCTT
XM_011514719.1:c.371+28726_371+28727insCTT XP_011513021.1:n.371+28726_371+28727insCTT
XR_926265.1:n.538+28726_538+28727insCTT
XR_926266.1:n.651+28726_651+28727insCTT
XR_926267.1:n.538+28726_538+28727insCTT
XM_011514719.2:c.371+28726_371+28727insCTT XP_011513021.1:n.371+28726_371+28727insCTT
XM_017010986.1:c.371+28726_371+28727insCTT XP_016866475.1:n.371+28726_371+28727insCTT
XM_017010987.1:c.-384+28726_-384+28727insCTT XP_016866476.1:n.-384+28726_-384+28727insCTT
XM_024446481.1:c.371+28726_371+28727insCTT XP_024302249.1:n.371+28726_371+28727insCTT
XR_001743495.2:n.543+28726_543+28727insCTT
XR_001743496.2:n.938+28726_938+28727insCTT
XR_001743500.1:n.538+28726_538+28727insCTT
XR_001743501.1:n.538+28726_538+28727insCTT
XR_926265.2:n.538+28726_538+28727insCTT
XR_926266.2:n.651+28726_651+28727insCTT
XR_926267.2:n.538+28726_538+28727insCTT