Canonical Allele Identifier: CA1062748716
Gene: CLOCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55460540G>A , CM000666.2:g.55460540G>A GRCh38
NC_000004.11:g.56326707G>A , CM000666.1:g.56326707G>A GRCh37
NC_000004.10:g.56021464G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000513440.6:c.560-1279C>T MANE Select ENSP00000426983.1:n.560-1279C>T
ENST00000309964.8:c.560-1279C>T ENSP00000308741.4:n.560-1279C>T
ENST00000381322.5:c.560-1279C>T ENSP00000370723.1:n.560-1279C>T
ENST00000506747.5:n.850-1279C>T
ENST00000513440.5:c.560-1279C>T ENSP00000426983.1:n.560-1279C>T
NM_001267843.1:c.560-1279C>T NP_001254772.1:n.560-1279C>T
NM_004898.3:c.560-1279C>T NP_004889.1:n.560-1279C>T
XM_005265787.1:c.560-1279C>T XP_005265844.1:n.560-1279C>T
XM_006714054.2:c.560-1279C>T XP_006714117.1:n.560-1279C>T
XM_011534409.1:c.560-1279C>T XP_011532711.1:n.560-1279C>T
XM_011534410.1:c.560-1279C>T XP_011532712.1:n.560-1279C>T
XM_011534411.1:c.560-1279C>T XP_011532713.1:n.560-1279C>T
XM_005265787.2:c.560-1279C>T XP_005265844.1:n.560-1279C>T
XM_011534409.2:c.560-1279C>T XP_011532711.1:n.560-1279C>T
XM_011534410.2:c.560-1279C>T XP_011532712.1:n.560-1279C>T
XM_011534411.2:c.560-1279C>T XP_011532713.1:n.560-1279C>T
XM_017008854.1:c.560-1279C>T XP_016864343.1:n.560-1279C>T
XM_017008855.1:c.383-1279C>T XP_016864344.1:n.383-1279C>T
XM_024454284.1:c.560-1279C>T XP_024310052.1:n.560-1279C>T
NM_004898.4:c.560-1279C>T MANE Select NP_004889.1:n.560-1279C>T
NM_001267843.2:c.560-1279C>T NP_001254772.1:n.560-1279C>T