Canonical Allele Identifier: CA2670685368

Gene: CLOCK TMEM165

Linked Data

• gnomAD v4: 4-55431938-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55431938C>A , CM000666.2:g.55431938C>A	GRCh38
NC_000004.11:g.56298105C>A , CM000666.1:g.56298105C>A	GRCh37
NC_000004.10:g.55992862C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000513440.6:c.*3477G>T (CLOCK) MANE Select	ENSP00000426983.1:n.*3477G>T
ENST00000309964.8:c.*3477G>T (CLOCK)	ENSP00000308741.4:n.*3477G>T
ENST00000506103.2:c.352+7295C>A (TMEM165)
ENST00000608091.1:c.408+7295C>A (TMEM165)
NM_001267843.1:c.*3477G>T (CLOCK)	NP_001254772.1:n.*3477G>T
NM_004898.3:c.*3477G>T (CLOCK)	NP_004889.1:n.*3477G>T
XM_005265787.1:c.*3477G>T (CLOCK)	XP_005265844.1:n.*3477G>T
XM_006714054.2:c.*3477G>T (CLOCK)	XP_006714117.1:n.*3477G>T
XM_011534394.1:c.898+7295C>A (TMEM165)	XP_011532696.1:n.898+7295C>A
XM_011534409.1:c.*3477G>T (CLOCK)	XP_011532711.1:n.*3477G>T
XM_011534410.1:c.*3477G>T (CLOCK)	XP_011532712.1:n.*3477G>T
XM_011534411.1:c.*3477G>T (CLOCK)	XP_011532713.1:n.*3477G>T
XM_005265787.2:c.*3477G>T (CLOCK)	XP_005265844.1:n.*3477G>T
XM_011534394.3:c.898+7295C>A (TMEM165)	XP_011532696.1:n.898+7295C>A
XM_011534409.2:c.*3477G>T (CLOCK)	XP_011532711.1:n.*3477G>T
XM_011534410.2:c.*3477G>T (CLOCK)	XP_011532712.1:n.*3477G>T
XM_011534411.2:c.*3477G>T (CLOCK)	XP_011532713.1:n.*3477G>T
XM_017008854.1:c.*3477G>T (CLOCK)	XP_016864343.1:n.*3477G>T
XM_017008855.1:c.*3477G>T (CLOCK)	XP_016864344.1:n.*3477G>T
XM_024454284.1:c.*3477G>T (CLOCK)	XP_024310052.1:n.*3477G>T
NM_004898.4:c.*3477G>T (CLOCK) MANE Select	NP_004889.1:n.*3477G>T
NM_001267843.2:c.*3477G>T (CLOCK)	NP_001254772.1:n.*3477G>T