Canonical Allele Identifier: CA2610514166
Gene: CHUK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100193877_100193880del , CM000672.2:g.100193877_100193880del GRCh38
NC_000010.10:g.101953634_101953637del , CM000672.1:g.101953634_101953637del GRCh37
NC_000010.9:g.101943624_101943627del NCBI36
NG_028023.1:g.40709_40712del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370397.8:c.1974+105_1974+108del MANE Select ENSP00000359424.6:n.1974+105_1974+108del
ENST00000370397.7:c.1974+105_1974+108del ENSP00000359424.6:n.1974+105_1974+108del
ENST00000588656.1:n.96+105_96+108del
ENST00000590930.5:n.2064_2067del
NM_001278.3:c.1974+105_1974+108del NP_001269.3:n.1974+105_1974+108del
XM_011539196.1:c.1974+105_1974+108del XP_011537498.1:n.1974+105_1974+108del
XM_011539197.1:c.1974+105_1974+108del XP_011537499.1:n.1974+105_1974+108del
XM_011539198.1:c.1974+105_1974+108del XP_011537500.1:n.1974+105_1974+108del
XR_945589.1:n.2052+105_2052+108del
NM_001278.4:c.1974+105_1974+108del NP_001269.3:n.1974+105_1974+108del
NM_001320928.1:c.1974+105_1974+108del NP_001307857.1:n.1974+105_1974+108del
XM_017015611.1:c.1974+105_1974+108del XP_016871100.1:n.1974+105_1974+108del
XM_017015613.1:c.762+105_762+108del XP_016871102.1:n.762+105_762+108del
XR_001747010.1:n.2052+105_2052+108del
XR_001747011.1:n.1949+105_1949+108del
NM_001278.5:c.1974+105_1974+108del MANE Select NP_001269.3:n.1974+105_1974+108del
NM_001320928.2:c.1974+105_1974+108del NP_001307857.1:n.1974+105_1974+108del