Canonical Allele Identifier: CA1931657455
Gene: CHUK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100216684A= , CM000672.2:g.100216684A= GRCh38
NC_000010.10:g.101976441A= , CM000672.1:g.101976441A= GRCh37
NC_000010.9:g.101966431A= NCBI36
NG_028023.1:g.17904T=

Transcript Alleles

HGVS Amino-acid change
ENST00000370397.8:c.933+1311T= MANE Select ENSP00000359424.6:n.933+1311T=
ENST00000370397.7:c.933+1311T= ENSP00000359424.6:n.933+1311T=
NM_001278.3:c.933+1311T= NP_001269.3:n.933+1311T=
XM_011539196.1:c.933+1311T= XP_011537498.1:n.933+1311T=
XM_011539197.1:c.933+1311T= XP_011537499.1:n.933+1311T=
XM_011539198.1:c.933+1311T= XP_011537500.1:n.933+1311T=
XR_945589.1:n.1011+1311T=
XR_945590.1:n.1011+1311T=
NM_001278.4:c.933+1311T= NP_001269.3:n.933+1311T=
NM_001320928.1:c.933+1311T= NP_001307857.1:n.933+1311T=
XM_017015611.1:c.933+1311T= XP_016871100.1:n.933+1311T=
XM_017015612.1:c.933+1311T= XP_016871101.1:n.933+1311T=
XR_001747010.1:n.1011+1311T=
XR_001747011.1:n.1011+1311T=
NM_001278.5:c.933+1311T= MANE Select NP_001269.3:n.933+1311T=
NM_001320928.2:c.933+1311T= NP_001307857.1:n.933+1311T=