Canonical Allele Identifier: CA2563326362

Gene: CLOCK

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55514382_55514383insCTTT , CM000666.2:g.55514382_55514383insCTTT	GRCh38
NC_000004.11:g.56380549_56380550insCTTT , CM000666.1:g.56380549_56380550insCTTT	GRCh37
NC_000004.10:g.56075306_56075307insCTTT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000513440.6:c.-289-4318_-289-4317insAAAG MANE Select	ENSP00000426983.1:n.-289-4318_-289-4317insAAAG
ENST00000381322.5:c.-446-4318_-446-4317insAAAG	ENSP00000370723.1:n.-446-4318_-446-4317insAAAG
ENST00000435527.6:c.-135-24918_-135-24917insAAAG	ENSP00000396649.2:n.-135-24918_-135-24917insAAAG
ENST00000506923.5:n.101-24918_101-24917insAAAG
ENST00000509151.5:n.175-4318_175-4317insAAAG
ENST00000513033.1:n.166-4318_166-4317insAAAG
ENST00000513440.5:c.-289-4318_-289-4317insAAAG	ENSP00000426983.1:n.-289-4318_-289-4317insAAAG
NM_001267843.1:c.-446-4318_-446-4317insAAAG	NP_001254772.1:n.-446-4318_-446-4317insAAAG
NM_004898.3:c.-289-4318_-289-4317insAAAG	NP_004889.1:n.-289-4318_-289-4317insAAAG
XM_005265787.1:c.-289-4318_-289-4317insAAAG	XP_005265844.1:n.-289-4318_-289-4317insAAAG
XM_006714054.2:c.-446-4318_-446-4317insAAAG	XP_006714117.1:n.-446-4318_-446-4317insAAAG
XM_011534409.1:c.-289-4318_-289-4317insAAAG	XP_011532711.1:n.-289-4318_-289-4317insAAAG
XM_011534410.1:c.-135-24918_-135-24917insAAAG	XP_011532712.1:n.-135-24918_-135-24917insAAAG
XM_011534411.1:c.-135-24918_-135-24917insAAAG	XP_011532713.1:n.-135-24918_-135-24917insAAAG
XM_005265787.2:c.-289-4318_-289-4317insAAAG	XP_005265844.1:n.-289-4318_-289-4317insAAAG
XM_011534409.2:c.-289-4318_-289-4317insAAAG	XP_011532711.1:n.-289-4318_-289-4317insAAAG
XM_011534410.2:c.-135-24918_-135-24917insAAAG	XP_011532712.1:n.-135-24918_-135-24917insAAAG
XM_011534411.2:c.-135-24918_-135-24917insAAAG	XP_011532713.1:n.-135-24918_-135-24917insAAAG
XM_017008854.1:c.-446-4318_-446-4317insAAAG	XP_016864343.1:n.-446-4318_-446-4317insAAAG
XM_024454284.1:c.-289-4318_-289-4317insAAAG	XP_024310052.1:n.-289-4318_-289-4317insAAAG
NM_004898.4:c.-289-4318_-289-4317insAAAG MANE Select	NP_004889.1:n.-289-4318_-289-4317insAAAG
NM_001267843.2:c.-446-4318_-446-4317insAAAG	NP_001254772.1:n.-446-4318_-446-4317insAAAG