Canonical Allele Identifier: CA1459119200

Gene: CLOCK

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55509814A= , CM000666.2:g.55509814A=	GRCh38
NC_000004.11:g.56375981A= , CM000666.1:g.56375981A=	GRCh37
NC_000004.10:g.56070738A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513440.6:c.-136+98T= MANE Select	ENSP00000426983.1:n.-136+98T=
ENST00000309964.8:c.-136+98T=	ENSP00000308741.4:n.-136+98T=
ENST00000381322.5:c.-293+98T=	ENSP00000370723.1:n.-293+98T=
ENST00000435527.6:c.-135-20349T=	ENSP00000396649.2:n.-135-20349T=
ENST00000506747.5:n.155+98T=
ENST00000506923.5:n.101-20349T=
ENST00000509151.5:n.328+98T=
ENST00000513033.1:n.319+98T=
ENST00000513440.5:c.-136+98T=	ENSP00000426983.1:n.-136+98T=
NM_001267843.1:c.-293+98T=	NP_001254772.1:n.-293+98T=
NM_004898.3:c.-136+98T=	NP_004889.1:n.-136+98T=
XM_005265787.1:c.-136+98T=	XP_005265844.1:n.-136+98T=
XM_006714054.2:c.-293+98T=	XP_006714117.1:n.-293+98T=
XM_011534409.1:c.-136+98T=	XP_011532711.1:n.-136+98T=
XM_011534410.1:c.-135-20349T=	XP_011532712.1:n.-135-20349T=
XM_011534411.1:c.-135-20349T=	XP_011532713.1:n.-135-20349T=
XM_005265787.2:c.-136+98T=	XP_005265844.1:n.-136+98T=
XM_011534409.2:c.-136+98T=	XP_011532711.1:n.-136+98T=
XM_011534410.2:c.-135-20349T=	XP_011532712.1:n.-135-20349T=
XM_011534411.2:c.-135-20349T=	XP_011532713.1:n.-135-20349T=
XM_017008854.1:c.-293+98T=	XP_016864343.1:n.-293+98T=
XM_024454284.1:c.-136+98T=	XP_024310052.1:n.-136+98T=
NM_004898.4:c.-136+98T= MANE Select	NP_004889.1:n.-136+98T=
NM_001267843.2:c.-293+98T=	NP_001254772.1:n.-293+98T=