Canonical Allele Identifier: CA595463903
Gene: CHUK HGNC NCBI

Linked Data

dbSNP Id: rs1457703222

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100216828del , CM000672.2:g.100216828del GRCh38
NC_000010.10:g.101976585del , CM000672.1:g.101976585del GRCh37
NC_000010.9:g.101966575del NCBI36
NG_028023.1:g.17760del

Transcript Alleles

HGVS Amino-acid change
ENST00000370397.8:c.933+1167del MANE Select ENSP00000359424.6:n.933+1167del
ENST00000370397.7:c.933+1167del ENSP00000359424.6:n.933+1167del
NM_001278.3:c.933+1167del NP_001269.3:n.933+1167del
XM_011539196.1:c.933+1167del XP_011537498.1:n.933+1167del
XM_011539197.1:c.933+1167del XP_011537499.1:n.933+1167del
XM_011539198.1:c.933+1167del XP_011537500.1:n.933+1167del
XR_945589.1:n.1011+1167del
XR_945590.1:n.1011+1167del
NM_001278.4:c.933+1167del NP_001269.3:n.933+1167del
NM_001320928.1:c.933+1167del NP_001307857.1:n.933+1167del
XM_017015611.1:c.933+1167del XP_016871100.1:n.933+1167del
XM_017015612.1:c.933+1167del XP_016871101.1:n.933+1167del
XR_001747010.1:n.1011+1167del
XR_001747011.1:n.1011+1167del
NM_001278.5:c.933+1167del MANE Select NP_001269.3:n.933+1167del
NM_001320928.2:c.933+1167del NP_001307857.1:n.933+1167del