Canonical Allele Identifier: CA1459075129

Gene: CLOCK TMEM165

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55443736G= , CM000666.2:g.55443736G=	GRCh38
NC_000004.11:g.56309903G= , CM000666.1:g.56309903G=	GRCh37
NC_000004.10:g.56004660G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513440.6:c.1853C= (CLOCK) MANE Select	ENSP00000426983.1:p.Thr618=
ENST00000309964.8:c.1853C= (CLOCK)	ENSP00000308741.4:p.Thr618=
ENST00000381322.5:c.1853C= (CLOCK)	ENSP00000370723.1:p.Thr618=
ENST00000479384.1:n.20C= (CLOCK)
ENST00000506103.2:c.353-8503G= (TMEM165)
ENST00000511124.1:n.435C= (CLOCK)
ENST00000513440.5:c.1853C= (CLOCK)	ENSP00000426983.1:p.Thr618=
ENST00000608091.1:c.409-8503G= (TMEM165)
NM_001267843.1:c.1853C= (CLOCK)	NP_001254772.1:p.Thr618=
NM_004898.3:c.1853C= (CLOCK)	NP_004889.1:p.Thr618=
XM_005265787.1:c.1853C= (CLOCK)	XP_005265844.1:p.Thr618=
XM_006714054.2:c.1853C= (CLOCK)	XP_006714117.1:p.Thr618=
XM_011534394.1:c.899-8503G= (TMEM165)	XP_011532696.1:n.899-8503G=
XM_011534409.1:c.1853C= (CLOCK)	XP_011532711.1:p.Thr618=
XM_011534410.1:c.1853C= (CLOCK)	XP_011532712.1:p.Thr618=
XM_011534411.1:c.1853C= (CLOCK)	XP_011532713.1:p.Thr618=
XM_005265787.2:c.1853C= (CLOCK)	XP_005265844.1:p.Thr618=
XM_011534394.3:c.899-8503G= (TMEM165)	XP_011532696.1:n.899-8503G=
XM_011534409.2:c.1853C= (CLOCK)	XP_011532711.1:p.Thr618=
XM_011534410.2:c.1853C= (CLOCK)	XP_011532712.1:p.Thr618=
XM_011534411.2:c.1853C= (CLOCK)	XP_011532713.1:p.Thr618=
XM_017008854.1:c.1853C= (CLOCK)	XP_016864343.1:p.Thr618=
XM_017008855.1:c.1676C= (CLOCK)	XP_016864344.1:p.Thr559=
XM_024454284.1:c.1853C= (CLOCK)	XP_024310052.1:p.Thr618=
NM_004898.4:c.1853C= (CLOCK) MANE Select	NP_004889.1:p.Thr618=
NM_001267843.2:c.1853C= (CLOCK)	NP_001254772.1:p.Thr618=