Canonical Allele Identifier: CA1459075279
Gene: CLOCK HGNC NCBI
TMEM165 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55443869_55443871delinsACC , CM000666.2:g.55443869_55443871delinsACC GRCh38
NC_000004.11:g.56310036_56310038delinsACC , CM000666.1:g.56310036_56310038delinsACC GRCh37
NC_000004.10:g.56004793_56004795delinsACC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000513440.6:c.1718_1720delinsGGT (CLOCK) MANE Select ENSP00000426983.1:p.Gly573=
ENST00000309964.8:c.1718_1720delinsGGT (CLOCK) ENSP00000308741.4:p.Gly573=
ENST00000381322.5:c.1718_1720delinsGGT (CLOCK) ENSP00000370723.1:p.Gly573=
ENST00000506103.2:c.353-8370_353-8368delinsACC (TMEM165)
ENST00000511124.1:n.300_302delinsGGT (CLOCK)
ENST00000513440.5:c.1718_1720delinsGGT (CLOCK) ENSP00000426983.1:p.Gly573=
ENST00000608091.1:c.409-8370_409-8368delinsACC (TMEM165)
NM_001267843.1:c.1718_1720delinsGGT (CLOCK) NP_001254772.1:p.Gly573=
NM_004898.3:c.1718_1720delinsGGT (CLOCK) NP_004889.1:p.Gly573=
XM_005265787.1:c.1718_1720delinsGGT (CLOCK) XP_005265844.1:p.Gly573=
XM_006714054.2:c.1718_1720delinsGGT (CLOCK) XP_006714117.1:p.Gly573=
XM_011534394.1:c.899-8370_899-8368delinsACC (TMEM165) XP_011532696.1:n.899-8370_899-8368delinsACC
XM_011534409.1:c.1718_1720delinsGGT (CLOCK) XP_011532711.1:p.Gly573=
XM_011534410.1:c.1718_1720delinsGGT (CLOCK) XP_011532712.1:p.Gly573=
XM_011534411.1:c.1718_1720delinsGGT (CLOCK) XP_011532713.1:p.Gly573=
XM_005265787.2:c.1718_1720delinsGGT (CLOCK) XP_005265844.1:p.Gly573=
XM_011534394.3:c.899-8370_899-8368delinsACC (TMEM165) XP_011532696.1:n.899-8370_899-8368delinsACC
XM_011534409.2:c.1718_1720delinsGGT (CLOCK) XP_011532711.1:p.Gly573=
XM_011534410.2:c.1718_1720delinsGGT (CLOCK) XP_011532712.1:p.Gly573=
XM_011534411.2:c.1718_1720delinsGGT (CLOCK) XP_011532713.1:p.Gly573=
XM_017008854.1:c.1718_1720delinsGGT (CLOCK) XP_016864343.1:p.Gly573=
XM_017008855.1:c.1541_1543delinsGGT (CLOCK) XP_016864344.1:p.Gly514=
XM_024454284.1:c.1718_1720delinsGGT (CLOCK) XP_024310052.1:p.Gly573=
NM_004898.4:c.1718_1720delinsGGT (CLOCK) MANE Select NP_004889.1:p.Gly573=
NM_001267843.2:c.1718_1720delinsGGT (CLOCK) NP_001254772.1:p.Gly573=