Canonical Allele Identifier: CA2610514251

Gene: CHUK

Linked Data

• gnomAD v4: 10-100193951-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100193951G>T , CM000672.2:g.100193951G>T	GRCh38
NC_000010.10:g.101953708G>T , CM000672.1:g.101953708G>T	GRCh37
NC_000010.9:g.101943698G>T	NCBI36
NG_028023.1:g.40637C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370397.8:c.1974+33C>A MANE Select	ENSP00000359424.6:n.1974+33C>A
ENST00000370397.7:c.1974+33C>A	ENSP00000359424.6:n.1974+33C>A
ENST00000588656.1:n.96+33C>A
ENST00000590930.5:n.1992C>A
NM_001278.3:c.1974+33C>A	NP_001269.3:n.1974+33C>A
XM_011539196.1:c.1974+33C>A	XP_011537498.1:n.1974+33C>A
XM_011539197.1:c.1974+33C>A	XP_011537499.1:n.1974+33C>A
XM_011539198.1:c.1974+33C>A	XP_011537500.1:n.1974+33C>A
XR_945589.1:n.2052+33C>A
NM_001278.4:c.1974+33C>A	NP_001269.3:n.1974+33C>A
NM_001320928.1:c.1974+33C>A	NP_001307857.1:n.1974+33C>A
XM_017015611.1:c.1974+33C>A	XP_016871100.1:n.1974+33C>A
XM_017015613.1:c.762+33C>A	XP_016871102.1:n.762+33C>A
XR_001747010.1:n.2052+33C>A
XR_001747011.1:n.1949+33C>A
NM_001278.5:c.1974+33C>A MANE Select	NP_001269.3:n.1974+33C>A
NM_001320928.2:c.1974+33C>A	NP_001307857.1:n.1974+33C>A