Canonical Allele Identifier: CA15327924
Gene: CLOCK HGNC NCBI
TMEM165 HGNC NCBI

Linked Data

dbSNP Id: rs2412646
gnomAD v2: 4-56318772-T-C
gnomAD v3: 4-55452605-T-C
gnomAD v4: 4-55452605-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55452605T>C , CM000666.2:g.55452605T>C GRCh38
NC_000004.11:g.56318772T>C , CM000666.1:g.56318772T>C GRCh37
NC_000004.10:g.56013529T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000513440.6:c.1206+449A>G (CLOCK) MANE Select ENSP00000426983.1:n.1206+449A>G
ENST00000309964.8:c.1206+449A>G (CLOCK) ENSP00000308741.4:n.1206+449A>G
ENST00000381322.5:c.1206+449A>G (CLOCK) ENSP00000370723.1:n.1206+449A>G
ENST00000513440.5:c.1206+449A>G (CLOCK) ENSP00000426983.1:n.1206+449A>G
ENST00000608091.1:c.775T>C (TMEM165)
NM_001267843.1:c.1206+449A>G (CLOCK) NP_001254772.1:n.1206+449A>G
NM_004898.3:c.1206+449A>G (CLOCK) NP_004889.1:n.1206+449A>G
XM_005265787.1:c.1206+449A>G (CLOCK) XP_005265844.1:n.1206+449A>G
XM_006714054.2:c.1206+449A>G (CLOCK) XP_006714117.1:n.1206+449A>G
XM_011534394.1:c.*299T>C (TMEM165) XP_011532696.1:n.*299T>C
XM_011534409.1:c.1206+449A>G (CLOCK) XP_011532711.1:n.1206+449A>G
XM_011534410.1:c.1206+449A>G (CLOCK) XP_011532712.1:n.1206+449A>G
XM_011534411.1:c.1206+449A>G (CLOCK) XP_011532713.1:n.1206+449A>G
XM_005265787.2:c.1206+449A>G (CLOCK) XP_005265844.1:n.1206+449A>G
XM_011534394.3:c.*299T>C (TMEM165) XP_011532696.1:n.*299T>C
XM_011534409.2:c.1206+449A>G (CLOCK) XP_011532711.1:n.1206+449A>G
XM_011534410.2:c.1206+449A>G (CLOCK) XP_011532712.1:n.1206+449A>G
XM_011534411.2:c.1206+449A>G (CLOCK) XP_011532713.1:n.1206+449A>G
XM_017008854.1:c.1206+449A>G (CLOCK) XP_016864343.1:n.1206+449A>G
XM_017008855.1:c.1029+449A>G (CLOCK) XP_016864344.1:n.1029+449A>G
XM_024454284.1:c.1206+449A>G (CLOCK) XP_024310052.1:n.1206+449A>G
NM_004898.4:c.1206+449A>G (CLOCK) MANE Select NP_004889.1:n.1206+449A>G
NM_001267843.2:c.1206+449A>G (CLOCK) NP_001254772.1:n.1206+449A>G