Canonical Allele Identifier: CA1931657606

Gene: CHUK

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100216827_100216828delinsAG , CM000672.2:g.100216827_100216828delinsAG	GRCh38
NC_000010.10:g.101976584_101976585delinsAG , CM000672.1:g.101976584_101976585delinsAG	GRCh37
NC_000010.9:g.101966574_101966575delinsAG	NCBI36
NG_028023.1:g.17760_17761delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000370397.8:c.933+1167_933+1168delinsCT MANE Select	ENSP00000359424.6:n.933+1167_933+1168deli...
ENST00000370397.7:c.933+1167_933+1168delinsCT	ENSP00000359424.6:n.933+1167_933+1168deli...
NM_001278.3:c.933+1167_933+1168delinsCT	NP_001269.3:n.933+1167_933+1168delinsCT
XM_011539196.1:c.933+1167_933+1168delinsCT	XP_011537498.1:n.933+1167_933+1168delinsC...
XM_011539197.1:c.933+1167_933+1168delinsCT	XP_011537499.1:n.933+1167_933+1168delinsC...
XM_011539198.1:c.933+1167_933+1168delinsCT	XP_011537500.1:n.933+1167_933+1168delinsC...
XR_945589.1:n.1011+1167_1011+1168delinsCT
XR_945590.1:n.1011+1167_1011+1168delinsCT
NM_001278.4:c.933+1167_933+1168delinsCT	NP_001269.3:n.933+1167_933+1168delinsCT
NM_001320928.1:c.933+1167_933+1168delinsCT	NP_001307857.1:n.933+1167_933+1168delinsC...
XM_017015611.1:c.933+1167_933+1168delinsCT	XP_016871100.1:n.933+1167_933+1168delinsC...
XM_017015612.1:c.933+1167_933+1168delinsCT	XP_016871101.1:n.933+1167_933+1168delinsC...
XR_001747010.1:n.1011+1167_1011+1168delinsCT
XR_001747011.1:n.1011+1167_1011+1168delinsCT
NM_001278.5:c.933+1167_933+1168delinsCT MANE Select	NP_001269.3:n.933+1167_933+1168delinsCT
NM_001320928.2:c.933+1167_933+1168delinsCT	NP_001307857.1:n.933+1167_933+1168delinsC...