Canonical Allele Identifier: CA1931657550

Gene: CHUK

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100216768G= , CM000672.2:g.100216768G=	GRCh38
NC_000010.10:g.101976525G= , CM000672.1:g.101976525G=	GRCh37
NC_000010.9:g.101966515G=	NCBI36
NG_028023.1:g.17820C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000370397.8:c.933+1227C= MANE Select	ENSP00000359424.6:n.933+1227C=
ENST00000370397.7:c.933+1227C=	ENSP00000359424.6:n.933+1227C=
NM_001278.3:c.933+1227C=	NP_001269.3:n.933+1227C=
XM_011539196.1:c.933+1227C=	XP_011537498.1:n.933+1227C=
XM_011539197.1:c.933+1227C=	XP_011537499.1:n.933+1227C=
XM_011539198.1:c.933+1227C=	XP_011537500.1:n.933+1227C=
XR_945589.1:n.1011+1227C=
XR_945590.1:n.1011+1227C=
NM_001278.4:c.933+1227C=	NP_001269.3:n.933+1227C=
NM_001320928.1:c.933+1227C=	NP_001307857.1:n.933+1227C=
XM_017015611.1:c.933+1227C=	XP_016871100.1:n.933+1227C=
XM_017015612.1:c.933+1227C=	XP_016871101.1:n.933+1227C=
XR_001747010.1:n.1011+1227C=
XR_001747011.1:n.1011+1227C=
NM_001278.5:c.933+1227C= MANE Select	NP_001269.3:n.933+1227C=
NM_001320928.2:c.933+1227C=	NP_001307857.1:n.933+1227C=