Canonical Allele Identifier: CA15326764
Gene: CLOCK HGNC NCBI
TMEM165 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1801260

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55435202A>G , CM000666.2:g.55435202A>G GRCh38
NC_000004.11:g.56301369A>G , CM000666.1:g.56301369A>G GRCh37
NC_000004.10:g.55996126A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001267843.1:c.*213T>C (CLOCK) VV NP_001254772.1:p.=
NM_004898.3:c.*213T>C (CLOCK) VV NP_004889.1:p.=
XM_005265787.1:c.*213T>C (CLOCK) XP_005265844.1:p.=
XM_006714054.2:c.*213T>C (CLOCK) XP_006714117.1:p.=
XM_011534394.1:c.898+10559A>G (TMEM165) XP_011532696.1:p.=
XM_011534409.1:c.*213T>C (CLOCK) XP_011532711.1:p.=
XM_011534410.1:c.*213T>C (CLOCK) XP_011532712.1:p.=
XM_011534411.1:c.*213T>C (CLOCK) XP_011532713.1:p.=
XM_005265787.2:c.*213T>C (CLOCK)
XM_011534394.3:c.898+10559A>G (TMEM165)
XM_011534409.2:c.*213T>C (CLOCK)
XM_011534410.2:c.*213T>C (CLOCK)
XM_011534411.2:c.*213T>C (CLOCK)
XM_017008854.1:c.*213T>C (CLOCK) XP_016864343.1:p.=
XM_017008855.1:c.*213T>C (CLOCK) XP_016864344.1:p.=
XM_024454284.1:c.*213T>C (CLOCK) XP_024310052.1:p.=
NM_004898.4:c.*213T>C (CLOCK) VV
ENST00000309964.8:c.*213T>C ENSP00000308741.4:p.=
ENST00000381322.5:c.*213T>C ENSP00000370723.1:p.=
ENST00000506103.2:n.352+10559A>G
ENST00000511124.1:n.1206T>C
ENST00000513440.5:c.*213T>C ENSP00000426983.1:p.=
ENST00000608091.1:n.408+10559A>G