Canonical Allele Identifier: CA16183424
Gene: CLOCK HGNC NCBI

Linked Data

dbSNP Id: rs12649507

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55514317G>A , CM000666.2:g.55514317G>A GRCh38
NC_000004.11:g.56380484G>A , CM000666.1:g.56380484G>A GRCh37
NC_000004.10:g.56075241G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000513440.6:c.-289-4252C>T MANE Select ENSP00000426983.1:p.=
ENST00000381322.5:c.-446-4252C>T ENSP00000370723.1:p.=
ENST00000435527.6:c.-135-24852C>T ENSP00000396649.2:p.=
ENST00000506923.5:n.101-24852C>T
ENST00000509151.5:n.175-4252C>T
ENST00000513033.1:n.166-4252C>T
ENST00000513440.5:c.-289-4252C>T ENSP00000426983.1:p.=
NM_001267843.1:c.-446-4252C>T NP_001254772.1:p.=
NM_004898.3:c.-289-4252C>T NP_004889.1:p.=
XM_005265787.1:c.-289-4252C>T XP_005265844.1:p.=
XM_006714054.2:c.-446-4252C>T XP_006714117.1:p.=
XM_011534409.1:c.-289-4252C>T XP_011532711.1:p.=
XM_011534410.1:c.-135-24852C>T XP_011532712.1:p.=
XM_011534411.1:c.-135-24852C>T XP_011532713.1:p.=
XM_005265787.2:c.-289-4252C>T XP_005265844.1:p.=
XM_011534409.2:c.-289-4252C>T XP_011532711.1:p.=
XM_011534410.2:c.-135-24852C>T XP_011532712.1:p.=
XM_011534411.2:c.-135-24852C>T XP_011532713.1:p.=
XM_017008854.1:c.-446-4252C>T XP_016864343.1:p.=
XM_024454284.1:c.-289-4252C>T XP_024310052.1:p.=
NM_004898.4:c.-289-4252C>T MANE Select NP_004889.1:p.=
NM_001267843.2:c.-446-4252C>T NP_001254772.1:p.=