Canonical Allele Identifier: CA471149304

Gene: CHUK

Linked Data

• MyVariant Identifiers: chr10:g.101953780T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100194023T>C , CM000672.2:g.100194023T>C	GRCh38
NC_000010.10:g.101953780T>C , CM000672.1:g.101953780T>C	GRCh37
NC_000010.9:g.101943770T>C	NCBI36
NG_028023.1:g.40565A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370397.8:c.1935A>G MANE Select	ENSP00000359424.6:p.Lys645=
ENST00000370397.7:c.1935A>G	ENSP00000359424.6:p.Lys645=
ENST00000588656.1:n.57A>G
ENST00000590930.5:n.1920A>G
NM_001278.3:c.1935A>G	NP_001269.3:p.Lys645=
XM_011539196.1:c.1935A>G	XP_011537498.1:p.Lys645=
XM_011539197.1:c.1935A>G	XP_011537499.1:p.Lys645=
XM_011539198.1:c.1935A>G	XP_011537500.1:p.Lys645=
XR_945589.1:n.2013A>G
NM_001278.4:c.1935A>G	NP_001269.3:p.Lys645=
NM_001320928.1:c.1935A>G	NP_001307857.1:p.Lys645=
XM_017015611.1:c.1935A>G	XP_016871100.1:p.Lys645=
XM_017015613.1:c.723A>G	XP_016871102.1:p.Lys241=
XR_001747010.1:n.2013A>G
XR_001747011.1:n.1910A>G
NM_001278.5:c.1935A>G MANE Select	NP_001269.3:p.Lys645=
NM_001320928.2:c.1935A>G	NP_001307857.1:p.Lys645=