Canonical Allele Identifier: CA439485226

Gene: CLOCK TMEM165

Linked Data

• MyVariant Identifiers: chr4:g.56309974A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55443807A>G , CM000666.2:g.55443807A>G	GRCh38
NC_000004.11:g.56309974A>G , CM000666.1:g.56309974A>G	GRCh37
NC_000004.10:g.56004731A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513440.6:c.1782T>C (CLOCK) MANE Select	ENSP00000426983.1:p.Pro594=
ENST00000309964.8:c.1782T>C (CLOCK)	ENSP00000308741.4:p.Pro594=
ENST00000381322.5:c.1782T>C (CLOCK)	ENSP00000370723.1:p.Pro594=
ENST00000506103.2:c.353-8432A>G (TMEM165)
ENST00000511124.1:n.364T>C (CLOCK)
ENST00000513440.5:c.1782T>C (CLOCK)	ENSP00000426983.1:p.Pro594=
ENST00000608091.1:c.409-8432A>G (TMEM165)
NM_001267843.1:c.1782T>C (CLOCK)	NP_001254772.1:p.Pro594=
NM_004898.3:c.1782T>C (CLOCK)	NP_004889.1:p.Pro594=
XM_005265787.1:c.1782T>C (CLOCK)	XP_005265844.1:p.Pro594=
XM_006714054.2:c.1782T>C (CLOCK)	XP_006714117.1:p.Pro594=
XM_011534394.1:c.899-8432A>G (TMEM165)	XP_011532696.1:n.899-8432A>G
XM_011534409.1:c.1782T>C (CLOCK)	XP_011532711.1:p.Pro594=
XM_011534410.1:c.1782T>C (CLOCK)	XP_011532712.1:p.Pro594=
XM_011534411.1:c.1782T>C (CLOCK)	XP_011532713.1:p.Pro594=
XM_005265787.2:c.1782T>C (CLOCK)	XP_005265844.1:p.Pro594=
XM_011534394.3:c.899-8432A>G (TMEM165)	XP_011532696.1:n.899-8432A>G
XM_011534409.2:c.1782T>C (CLOCK)	XP_011532711.1:p.Pro594=
XM_011534410.2:c.1782T>C (CLOCK)	XP_011532712.1:p.Pro594=
XM_011534411.2:c.1782T>C (CLOCK)	XP_011532713.1:p.Pro594=
XM_017008854.1:c.1782T>C (CLOCK)	XP_016864343.1:p.Pro594=
XM_017008855.1:c.1605T>C (CLOCK)	XP_016864344.1:p.Pro535=
XM_024454284.1:c.1782T>C (CLOCK)	XP_024310052.1:p.Pro594=
NM_004898.4:c.1782T>C (CLOCK) MANE Select	NP_004889.1:p.Pro594=
NM_001267843.2:c.1782T>C (CLOCK)	NP_001254772.1:p.Pro594=