Canonical Allele Identifier: CA16256062
Gene: CDKAL1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10440833

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.20687890T>A , CM000668.2:g.20687890T>A GRCh38
NC_000006.11:g.20688121T>A , CM000668.1:g.20688121T>A GRCh37
NC_000006.10:g.20796100T>A NCBI36
NG_021195.1:g.158434T>A
NG_021195.2:g.158434T>A

Transcript Alleles

HGVS Amino-acid change
NM_017774.3:c.371+38513T>A VV MANE Preferred NP_060244.2:p.=
XM_006715128.2:c.371+38513T>A XP_006715191.1:p.=
XM_011514718.1:c.371+38513T>A XP_011513020.1:p.=
XM_011514719.1:c.371+38513T>A XP_011513021.1:p.=
XR_926265.1:n.538+38513T>A
XR_926266.1:n.651+38513T>A
XR_926267.1:n.538+38513T>A
XM_011514719.2:c.371+38513T>A XP_011513021.1:p.=
XM_017010986.1:c.371+38513T>A XP_016866475.1:p.=
XM_017010987.1:c.-384+38513T>A XP_016866476.1:p.=
XM_024446481.1:c.371+38513T>A XP_024302249.1:p.=
XR_001743495.2:n.543+38513T>A
XR_001743496.2:n.938+38513T>A
XR_001743500.1:n.538+38513T>A
XR_001743501.1:n.538+38513T>A
XR_926265.2:n.538+38513T>A
XR_926266.2:n.651+38513T>A
XR_926267.2:n.538+38513T>A
ENST00000274695.8:c.371+38513T>A ENSP00000274695.4:p.=
ENST00000378610.1:c.371+38513T>A ENSP00000367873.1:p.=