Canonical Allele Identifier: CA2656677430

Gene: CSNK1E TPTEP2-CSNK1E

Linked Data

• gnomAD v4: 22-38299075-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38299075A>G , CM000684.2:g.38299075A>G	GRCh38
NC_000022.10:g.38695080A>G , CM000684.1:g.38695080A>G	GRCh37
NC_000022.9:g.37025026A>G	NCBI36
NG_016707.1:g.24010T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000396832.6:c.737-141T>C (CSNK1E) MANE Select	ENSP00000380044.1:n.737-141T>C
ENST00000400206.7:c.737-141T>C (TPTEP2-CSNK1E)	ENSP00000383067.2:n.737-141T>C
ENST00000612795.2:c.531-141T>C (CSNK1E)
ENST00000359867.7:c.737-141T>C (CSNK1E)	ENSP00000352929.3:n.737-141T>C
ENST00000396832.5:c.737-141T>C (CSNK1E)	ENSP00000380044.1:n.737-141T>C
ENST00000400206.6:c.737-141T>C (CSNK1E)	ENSP00000383067.2:n.737-141T>C
ENST00000403904.5:c.737-141T>C (CSNK1E)	ENSP00000384074.1:n.737-141T>C
ENST00000405675.7:c.737-141T>C (CSNK1E)	ENSP00000384426.3:n.737-141T>C
ENST00000413574.6:c.737-141T>C (CSNK1E)	ENSP00000407235.2:n.737-141T>C
ENST00000431611.5:c.212-141T>C (CSNK1E)
ENST00000442216.1:c.132-141T>C (CSNK1E)
ENST00000451964.5:c.550-141T>C (CSNK1E)
ENST00000498529.5:n.172-141T>C (CSNK1E)
ENST00000612795.1:n.531-141T>C (CSNK1E)
NM_001289912.1:c.737-141T>C (TPTEP2-CSNK1E)	NP_001276841.1:n.737-141T>C
NM_001894.4:c.737-141T>C (CSNK1E)	NP_001885.1:n.737-141T>C
NM_152221.2:c.737-141T>C (CSNK1E)	NP_689407.1:n.737-141T>C
NM_152221.3:c.737-141T>C (CSNK1E) MANE Select	NP_689407.1:n.737-141T>C
NM_001289912.2:c.737-141T>C (TPTEP2-CSNK1E)	NP_001276841.1:n.737-141T>C
NM_001894.5:c.737-141T>C (CSNK1E)	NP_001885.1:n.737-141T>C