Canonical Allele Identifier: CA11646887
Gene: CLOCK HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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