Canonical Allele Identifier: CA1931630868

Gene: CHUK

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100194002A= , CM000672.2:g.100194002A=	GRCh38
NC_000010.10:g.101953759A= , CM000672.1:g.101953759A=	GRCh37
NC_000010.9:g.101943749A=	NCBI36
NG_028023.1:g.40586T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370397.8:c.1956T= MANE Select	ENSP00000359424.6:p.His652=
ENST00000370397.7:c.1956T=	ENSP00000359424.6:p.His652=
ENST00000588656.1:n.78T=
ENST00000590930.5:n.1941T=
NM_001278.3:c.1956T=	NP_001269.3:p.His652=
XM_011539196.1:c.1956T=	XP_011537498.1:p.His652=
XM_011539197.1:c.1956T=	XP_011537499.1:p.His652=
XM_011539198.1:c.1956T=	XP_011537500.1:p.His652=
XR_945589.1:n.2034T=
NM_001278.4:c.1956T=	NP_001269.3:p.His652=
NM_001320928.1:c.1956T=	NP_001307857.1:p.His652=
XM_017015611.1:c.1956T=	XP_016871100.1:p.His652=
XM_017015613.1:c.744T=	XP_016871102.1:p.His248=
XR_001747010.1:n.2034T=
XR_001747011.1:n.1931T=
NM_001278.5:c.1956T= MANE Select	NP_001269.3:p.His652=
NM_001320928.2:c.1956T=	NP_001307857.1:p.His652=