Canonical Allele Identifier: CA11751361

Gene: CLOCK

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55455650C>G , CM000666.2:g.55455650C>G	GRCh38
NC_000004.11:g.56321817C>G , CM000666.1:g.56321817C>G	GRCh37
NC_000004.10:g.56016574C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513440.6:c.982+247G>C MANE Select	ENSP00000426983.1:n.982+247G>C
ENST00000309964.8:c.982+247G>C	ENSP00000308741.4:n.982+247G>C
ENST00000381322.5:c.982+247G>C	ENSP00000370723.1:n.982+247G>C
ENST00000506747.5:n.1272+247G>C
ENST00000513440.5:c.982+247G>C	ENSP00000426983.1:n.982+247G>C
NM_001267843.1:c.982+247G>C	NP_001254772.1:n.982+247G>C
NM_004898.3:c.982+247G>C	NP_004889.1:n.982+247G>C
XM_005265787.1:c.982+247G>C	XP_005265844.1:n.982+247G>C
XM_006714054.2:c.982+247G>C	XP_006714117.1:n.982+247G>C
XM_011534409.1:c.982+247G>C	XP_011532711.1:n.982+247G>C
XM_011534410.1:c.982+247G>C	XP_011532712.1:n.982+247G>C
XM_011534411.1:c.982+247G>C	XP_011532713.1:n.982+247G>C
XM_005265787.2:c.982+247G>C	XP_005265844.1:n.982+247G>C
XM_011534409.2:c.982+247G>C	XP_011532711.1:n.982+247G>C
XM_011534410.2:c.982+247G>C	XP_011532712.1:n.982+247G>C
XM_011534411.2:c.982+247G>C	XP_011532713.1:n.982+247G>C
XM_017008854.1:c.982+247G>C	XP_016864343.1:n.982+247G>C
XM_017008855.1:c.805+247G>C	XP_016864344.1:n.805+247G>C
XM_024454284.1:c.982+247G>C	XP_024310052.1:n.982+247G>C
NM_004898.4:c.982+247G>C MANE Select	NP_004889.1:n.982+247G>C
NM_001267843.2:c.982+247G>C	NP_001254772.1:n.982+247G>C