Canonical Allele Identifier: CA1931630920

Gene: CHUK

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100194050G= , CM000672.2:g.100194050G=	GRCh38
NC_000010.10:g.101953807G= , CM000672.1:g.101953807G=	GRCh37
NC_000010.9:g.101943797G=	NCBI36
NG_028023.1:g.40538C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370397.8:c.1908C= MANE Select	ENSP00000359424.6:p.Asp636=
ENST00000370397.7:c.1908C=	ENSP00000359424.6:p.Asp636=
ENST00000588656.1:n.30C=
ENST00000590930.5:n.1893C=
NM_001278.3:c.1908C=	NP_001269.3:p.Asp636=
XM_011539196.1:c.1908C=	XP_011537498.1:p.Asp636=
XM_011539197.1:c.1908C=	XP_011537499.1:p.Asp636=
XM_011539198.1:c.1908C=	XP_011537500.1:p.Asp636=
XR_945589.1:n.1986C=
NM_001278.4:c.1908C=	NP_001269.3:p.Asp636=
NM_001320928.1:c.1908C=	NP_001307857.1:p.Asp636=
XM_017015611.1:c.1908C=	XP_016871100.1:p.Asp636=
XM_017015613.1:c.696C=	XP_016871102.1:p.Asp232=
XR_001747010.1:n.1986C=
XR_001747011.1:n.1883C=
NM_001278.5:c.1908C= MANE Select	NP_001269.3:p.Asp636=
NM_001320928.2:c.1908C=	NP_001307857.1:p.Asp636=