Canonical Allele Identifier: CA96895979
Gene: CLOCK HGNC NCBI
TMEM165 HGNC NCBI

Linked Data

dbSNP Id: rs764290289
gnomAD v2: 4-56301327-T-C
gnomAD v3: 4-55435160-T-C
gnomAD v4: 4-55435160-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55435160T>C , CM000666.2:g.55435160T>C GRCh38
NC_000004.11:g.56301327T>C , CM000666.1:g.56301327T>C GRCh37
NC_000004.10:g.55996084T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000513440.6:c.*255A>G (CLOCK) MANE Select ENSP00000426983.1:n.*255A>G
ENST00000309964.8:c.*255A>G (CLOCK) ENSP00000308741.4:n.*255A>G
ENST00000381322.5:c.*255A>G (CLOCK) ENSP00000370723.1:n.*255A>G
ENST00000506103.2:c.352+10517T>C (TMEM165)
ENST00000511124.1:n.1248A>G (CLOCK)
ENST00000513440.5:c.*255A>G (CLOCK) ENSP00000426983.1:n.*255A>G
ENST00000608091.1:c.408+10517T>C (TMEM165)
NM_001267843.1:c.*255A>G (CLOCK) NP_001254772.1:n.*255A>G
NM_004898.3:c.*255A>G (CLOCK) NP_004889.1:n.*255A>G
XM_005265787.1:c.*255A>G (CLOCK) XP_005265844.1:n.*255A>G
XM_006714054.2:c.*255A>G (CLOCK) XP_006714117.1:n.*255A>G
XM_011534394.1:c.898+10517T>C (TMEM165) XP_011532696.1:n.898+10517T>C
XM_011534409.1:c.*255A>G (CLOCK) XP_011532711.1:n.*255A>G
XM_011534410.1:c.*255A>G (CLOCK) XP_011532712.1:n.*255A>G
XM_011534411.1:c.*255A>G (CLOCK) XP_011532713.1:n.*255A>G
XM_005265787.2:c.*255A>G (CLOCK) XP_005265844.1:n.*255A>G
XM_011534394.3:c.898+10517T>C (TMEM165) XP_011532696.1:n.898+10517T>C
XM_011534409.2:c.*255A>G (CLOCK) XP_011532711.1:n.*255A>G
XM_011534410.2:c.*255A>G (CLOCK) XP_011532712.1:n.*255A>G
XM_011534411.2:c.*255A>G (CLOCK) XP_011532713.1:n.*255A>G
XM_017008854.1:c.*255A>G (CLOCK) XP_016864343.1:n.*255A>G
XM_017008855.1:c.*255A>G (CLOCK) XP_016864344.1:n.*255A>G
XM_024454284.1:c.*255A>G (CLOCK) XP_024310052.1:n.*255A>G
NM_004898.4:c.*255A>G (CLOCK) MANE Select NP_004889.1:n.*255A>G
NM_001267843.2:c.*255A>G (CLOCK) NP_001254772.1:n.*255A>G