Canonical Allele Identifier: CA2670687052

Gene: CLOCK TMEM165

Linked Data

• gnomAD v4: 4-55435046-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55435046T>C , CM000666.2:g.55435046T>C	GRCh38
NC_000004.11:g.56301213T>C , CM000666.1:g.56301213T>C	GRCh37
NC_000004.10:g.55995970T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513440.6:c.*369A>G (CLOCK) MANE Select	ENSP00000426983.1:n.*369A>G
ENST00000309964.8:c.*369A>G (CLOCK)	ENSP00000308741.4:n.*369A>G
ENST00000381322.5:c.*369A>G (CLOCK)	ENSP00000370723.1:n.*369A>G
ENST00000506103.2:c.352+10403T>C (TMEM165)
ENST00000511124.1:n.1362A>G (CLOCK)
ENST00000513440.5:c.*369A>G (CLOCK)	ENSP00000426983.1:n.*369A>G
ENST00000608091.1:c.408+10403T>C (TMEM165)
NM_001267843.1:c.*369A>G (CLOCK)	NP_001254772.1:n.*369A>G
NM_004898.3:c.*369A>G (CLOCK)	NP_004889.1:n.*369A>G
XM_005265787.1:c.*369A>G (CLOCK)	XP_005265844.1:n.*369A>G
XM_006714054.2:c.*369A>G (CLOCK)	XP_006714117.1:n.*369A>G
XM_011534394.1:c.898+10403T>C (TMEM165)	XP_011532696.1:n.898+10403T>C
XM_011534409.1:c.*369A>G (CLOCK)	XP_011532711.1:n.*369A>G
XM_011534410.1:c.*369A>G (CLOCK)	XP_011532712.1:n.*369A>G
XM_011534411.1:c.*369A>G (CLOCK)	XP_011532713.1:n.*369A>G
XM_005265787.2:c.*369A>G (CLOCK)	XP_005265844.1:n.*369A>G
XM_011534394.3:c.898+10403T>C (TMEM165)	XP_011532696.1:n.898+10403T>C
XM_011534409.2:c.*369A>G (CLOCK)	XP_011532711.1:n.*369A>G
XM_011534410.2:c.*369A>G (CLOCK)	XP_011532712.1:n.*369A>G
XM_011534411.2:c.*369A>G (CLOCK)	XP_011532713.1:n.*369A>G
XM_017008854.1:c.*369A>G (CLOCK)	XP_016864343.1:n.*369A>G
XM_017008855.1:c.*369A>G (CLOCK)	XP_016864344.1:n.*369A>G
XM_024454284.1:c.*369A>G (CLOCK)	XP_024310052.1:n.*369A>G
NM_004898.4:c.*369A>G (CLOCK) MANE Select	NP_004889.1:n.*369A>G
NM_001267843.2:c.*369A>G (CLOCK)	NP_001254772.1:n.*369A>G