Canonical Allele Identifier: CA471149294

Gene: CHUK

Linked Data

• gnomAD v4: 10-100194014-T-C
• MyVariant Identifiers: chr10:g.101953771T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100194014T>C , CM000672.2:g.100194014T>C	GRCh38
NC_000010.10:g.101953771T>C , CM000672.1:g.101953771T>C	GRCh37
NC_000010.9:g.101943761T>C	NCBI36
NG_028023.1:g.40574A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370397.8:c.1944A>G MANE Select	ENSP00000359424.6:p.Lys648=
ENST00000370397.7:c.1944A>G	ENSP00000359424.6:p.Lys648=
ENST00000588656.1:n.66A>G
ENST00000590930.5:n.1929A>G
NM_001278.3:c.1944A>G	NP_001269.3:p.Lys648=
XM_011539196.1:c.1944A>G	XP_011537498.1:p.Lys648=
XM_011539197.1:c.1944A>G	XP_011537499.1:p.Lys648=
XM_011539198.1:c.1944A>G	XP_011537500.1:p.Lys648=
XR_945589.1:n.2022A>G
NM_001278.4:c.1944A>G	NP_001269.3:p.Lys648=
NM_001320928.1:c.1944A>G	NP_001307857.1:p.Lys648=
XM_017015611.1:c.1944A>G	XP_016871100.1:p.Lys648=
XM_017015613.1:c.732A>G	XP_016871102.1:p.Lys244=
XR_001747010.1:n.2022A>G
XR_001747011.1:n.1919A>G
NM_001278.5:c.1944A>G MANE Select	NP_001269.3:p.Lys648=
NM_001320928.2:c.1944A>G	NP_001307857.1:p.Lys648=