Canonical Allele Identifier: CA471149296

Gene: CHUK

Linked Data

• MyVariant Identifiers: chr10:g.101953774C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100194017C>T , CM000672.2:g.100194017C>T	GRCh38
NC_000010.10:g.101953774C>T , CM000672.1:g.101953774C>T	GRCh37
NC_000010.9:g.101943764C>T	NCBI36
NG_028023.1:g.40571G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370397.8:c.1941G>A MANE Select	ENSP00000359424.6:p.Gln647=
ENST00000370397.7:c.1941G>A	ENSP00000359424.6:p.Gln647=
ENST00000588656.1:n.63G>A
ENST00000590930.5:n.1926G>A
NM_001278.3:c.1941G>A	NP_001269.3:p.Gln647=
XM_011539196.1:c.1941G>A	XP_011537498.1:p.Gln647=
XM_011539197.1:c.1941G>A	XP_011537499.1:p.Gln647=
XM_011539198.1:c.1941G>A	XP_011537500.1:p.Gln647=
XR_945589.1:n.2019G>A
NM_001278.4:c.1941G>A	NP_001269.3:p.Gln647=
NM_001320928.1:c.1941G>A	NP_001307857.1:p.Gln647=
XM_017015611.1:c.1941G>A	XP_016871100.1:p.Gln647=
XM_017015613.1:c.729G>A	XP_016871102.1:p.Gln243=
XR_001747010.1:n.2019G>A
XR_001747011.1:n.1916G>A
NM_001278.5:c.1941G>A MANE Select	NP_001269.3:p.Gln647=
NM_001320928.2:c.1941G>A	NP_001307857.1:p.Gln647=