Canonical Allele Identifier: CA356915405

Gene: CLOCK TMEM165

Linked Data

• MyVariant Identifiers: chr4:g.56309938C>A (hg19) ; chr4:g.55443771C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55443771C>A , CM000666.2:g.55443771C>A	GRCh38
NC_000004.11:g.56309938C>A , CM000666.1:g.56309938C>A	GRCh37
NC_000004.10:g.56004695C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513440.6:c.1818G>T (CLOCK) MANE Select	ENSP00000426983.1:p.Gln606His
ENST00000309964.8:c.1818G>T (CLOCK)	ENSP00000308741.4:p.Gln606His
ENST00000381322.5:c.1818G>T (CLOCK)	ENSP00000370723.1:p.Gln606His
ENST00000506103.2:c.353-8468C>A (TMEM165)
ENST00000511124.1:n.400G>T (CLOCK)
ENST00000513440.5:c.1818G>T (CLOCK)	ENSP00000426983.1:p.Gln606His
ENST00000608091.1:c.409-8468C>A (TMEM165)
NM_001267843.1:c.1818G>T (CLOCK)	NP_001254772.1:p.Gln606His
NM_004898.3:c.1818G>T (CLOCK)	NP_004889.1:p.Gln606His
XM_005265787.1:c.1818G>T (CLOCK)	XP_005265844.1:p.Gln606His
XM_006714054.2:c.1818G>T (CLOCK)	XP_006714117.1:p.Gln606His
XM_011534394.1:c.899-8468C>A (TMEM165)	XP_011532696.1:n.899-8468C>A
XM_011534409.1:c.1818G>T (CLOCK)	XP_011532711.1:p.Gln606His
XM_011534410.1:c.1818G>T (CLOCK)	XP_011532712.1:p.Gln606His
XM_011534411.1:c.1818G>T (CLOCK)	XP_011532713.1:p.Gln606His
XM_005265787.2:c.1818G>T (CLOCK)	XP_005265844.1:p.Gln606His
XM_011534394.3:c.899-8468C>A (TMEM165)	XP_011532696.1:n.899-8468C>A
XM_011534409.2:c.1818G>T (CLOCK)	XP_011532711.1:p.Gln606His
XM_011534410.2:c.1818G>T (CLOCK)	XP_011532712.1:p.Gln606His
XM_011534411.2:c.1818G>T (CLOCK)	XP_011532713.1:p.Gln606His
XM_017008854.1:c.1818G>T (CLOCK)	XP_016864343.1:p.Gln606His
XM_017008855.1:c.1641G>T (CLOCK)	XP_016864344.1:p.Gln547His
XM_024454284.1:c.1818G>T (CLOCK)	XP_024310052.1:p.Gln606His
NM_004898.4:c.1818G>T (CLOCK) MANE Select	NP_004889.1:p.Gln606His
NM_001267843.2:c.1818G>T (CLOCK)	NP_001254772.1:p.Gln606His