Canonical Allele Identifier: CA411523624

Gene: CSNK1E TPTEP2-CSNK1E

Linked Data

• MyVariant Identifiers: chr22:g.38694826A>C (hg19) ; chr22:g.38298821A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38298821A>C , CM000684.2:g.38298821A>C	GRCh38
NC_000022.10:g.38694826A>C , CM000684.1:g.38694826A>C	GRCh37
NC_000022.9:g.37024772A>C	NCBI36
NG_016707.1:g.24264T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396832.6:c.850T>G (CSNK1E) MANE Select	ENSP00000380044.1:p.Tyr284Asp
ENST00000400206.7:c.850T>G (TPTEP2-CSNK1E)	ENSP00000383067.2:p.Tyr284Asp
ENST00000612795.2:c.644T>G (CSNK1E)
ENST00000359867.7:c.850T>G (CSNK1E)	ENSP00000352929.3:p.Tyr284Asp
ENST00000396832.5:c.850T>G (CSNK1E)	ENSP00000380044.1:p.Tyr284Asp
ENST00000400206.6:c.850T>G (CSNK1E)	ENSP00000383067.2:p.Tyr284Asp
ENST00000403904.5:c.850T>G (CSNK1E)	ENSP00000384074.1:p.Tyr284Asp
ENST00000405675.7:c.850T>G (CSNK1E)	ENSP00000384426.3:p.Tyr284Asp
ENST00000413574.6:c.850T>G (CSNK1E)	ENSP00000407235.2:p.Tyr284Asp
ENST00000431611.5:c.325T>G (CSNK1E)
ENST00000431632.5:c.32T>G (CSNK1E)
ENST00000442216.1:c.245T>G (CSNK1E)
ENST00000451964.5:c.663T>G (CSNK1E)
ENST00000498529.5:n.285T>G (CSNK1E)
ENST00000612795.1:n.644T>G (CSNK1E)
NM_001289912.1:c.850T>G (TPTEP2-CSNK1E)	NP_001276841.1:p.Tyr284Asp
NM_001894.4:c.850T>G (CSNK1E)	NP_001885.1:p.Tyr284Asp
NM_152221.2:c.850T>G (CSNK1E)	NP_689407.1:p.Tyr284Asp
NM_152221.3:c.850T>G (CSNK1E) MANE Select	NP_689407.1:p.Tyr284Asp
NM_001289912.2:c.850T>G (TPTEP2-CSNK1E)	NP_001276841.1:p.Tyr284Asp
NM_001894.5:c.850T>G (CSNK1E)	NP_001885.1:p.Tyr284Asp