Canonical Allele Identifier: CA1459122707

Gene: CLOCK

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55514388C= , CM000666.2:g.55514388C=	GRCh38
NC_000004.11:g.56380555C= , CM000666.1:g.56380555C=	GRCh37
NC_000004.10:g.56075312C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000513440.6:c.-289-4323G= MANE Select	ENSP00000426983.1:n.-289-4323G=
ENST00000381322.5:c.-446-4323G=	ENSP00000370723.1:n.-446-4323G=
ENST00000435527.6:c.-135-24923G=	ENSP00000396649.2:n.-135-24923G=
ENST00000506923.5:n.101-24923G=
ENST00000509151.5:n.175-4323G=
ENST00000513033.1:n.166-4323G=
ENST00000513440.5:c.-289-4323G=	ENSP00000426983.1:n.-289-4323G=
NM_001267843.1:c.-446-4323G=	NP_001254772.1:n.-446-4323G=
NM_004898.3:c.-289-4323G=	NP_004889.1:n.-289-4323G=
XM_005265787.1:c.-289-4323G=	XP_005265844.1:n.-289-4323G=
XM_006714054.2:c.-446-4323G=	XP_006714117.1:n.-446-4323G=
XM_011534409.1:c.-289-4323G=	XP_011532711.1:n.-289-4323G=
XM_011534410.1:c.-135-24923G=	XP_011532712.1:n.-135-24923G=
XM_011534411.1:c.-135-24923G=	XP_011532713.1:n.-135-24923G=
XM_005265787.2:c.-289-4323G=	XP_005265844.1:n.-289-4323G=
XM_011534409.2:c.-289-4323G=	XP_011532711.1:n.-289-4323G=
XM_011534410.2:c.-135-24923G=	XP_011532712.1:n.-135-24923G=
XM_011534411.2:c.-135-24923G=	XP_011532713.1:n.-135-24923G=
XM_017008854.1:c.-446-4323G=	XP_016864343.1:n.-446-4323G=
XM_024454284.1:c.-289-4323G=	XP_024310052.1:n.-289-4323G=
NM_004898.4:c.-289-4323G= MANE Select	NP_004889.1:n.-289-4323G=
NM_001267843.2:c.-446-4323G=	NP_001254772.1:n.-446-4323G=