Canonical Allele Identifier: CA1459122686
Gene: CLOCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55514351_55514352delinsAC , CM000666.2:g.55514351_55514352delinsAC GRCh38
NC_000004.11:g.56380518_56380519delinsAC , CM000666.1:g.56380518_56380519delinsAC GRCh37
NC_000004.10:g.56075275_56075276delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000513440.6:c.-289-4287_-289-4286delinsGT MANE Select ENSP00000426983.1:n.-289-4287_-289-4286de...
ENST00000381322.5:c.-446-4287_-446-4286delinsGT ENSP00000370723.1:n.-446-4287_-446-4286de...
ENST00000435527.6:c.-135-24887_-135-24886delinsGT ENSP00000396649.2:n.-135-24887_-135-24886...
ENST00000506923.5:n.101-24887_101-24886delinsGT
ENST00000509151.5:n.175-4287_175-4286delinsGT
ENST00000513033.1:n.166-4287_166-4286delinsGT
ENST00000513440.5:c.-289-4287_-289-4286delinsGT ENSP00000426983.1:n.-289-4287_-289-4286de...
NM_001267843.1:c.-446-4287_-446-4286delinsGT NP_001254772.1:n.-446-4287_-446-4286delin...
NM_004898.3:c.-289-4287_-289-4286delinsGT NP_004889.1:n.-289-4287_-289-4286delinsGT...
XM_005265787.1:c.-289-4287_-289-4286delinsGT XP_005265844.1:n.-289-4287_-289-4286delin...
XM_006714054.2:c.-446-4287_-446-4286delinsGT XP_006714117.1:n.-446-4287_-446-4286delin...
XM_011534409.1:c.-289-4287_-289-4286delinsGT XP_011532711.1:n.-289-4287_-289-4286delin...
XM_011534410.1:c.-135-24887_-135-24886delinsGT XP_011532712.1:n.-135-24887_-135-24886del...
XM_011534411.1:c.-135-24887_-135-24886delinsGT XP_011532713.1:n.-135-24887_-135-24886del...
XM_005265787.2:c.-289-4287_-289-4286delinsGT XP_005265844.1:n.-289-4287_-289-4286delin...
XM_011534409.2:c.-289-4287_-289-4286delinsGT XP_011532711.1:n.-289-4287_-289-4286delin...
XM_011534410.2:c.-135-24887_-135-24886delinsGT XP_011532712.1:n.-135-24887_-135-24886del...
XM_011534411.2:c.-135-24887_-135-24886delinsGT XP_011532713.1:n.-135-24887_-135-24886del...
XM_017008854.1:c.-446-4287_-446-4286delinsGT XP_016864343.1:n.-446-4287_-446-4286delin...
XM_024454284.1:c.-289-4287_-289-4286delinsGT XP_024310052.1:n.-289-4287_-289-4286delin...
NM_004898.4:c.-289-4287_-289-4286delinsGT MANE Select NP_004889.1:n.-289-4287_-289-4286delinsGT...
NM_001267843.2:c.-446-4287_-446-4286delinsGT NP_001254772.1:n.-446-4287_-446-4286delin...