Canonical Allele Identifier: CA15639265
Gene: CHUK HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11591741

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100216744G>C , CM000672.2:g.100216744G>C GRCh38
NC_000010.10:g.101976501G>C , CM000672.1:g.101976501G>C GRCh37
NC_000010.9:g.101966491G>C NCBI36
NG_028023.1:g.17844C>G

Transcript Alleles

HGVS Amino-acid change
NM_001278.3:c.933+1251C>G VV NP_001269.3:p.=
XM_011539196.1:c.933+1251C>G XP_011537498.1:p.=
XM_011539197.1:c.933+1251C>G XP_011537499.1:p.=
XM_011539198.1:c.933+1251C>G XP_011537500.1:p.=
XR_945589.1:n.1011+1251C>G
XR_945590.1:n.1011+1251C>G
NM_001278.4:c.933+1251C>G VV
NM_001320928.1:c.933+1251C>G VV NP_001307857.1:p.=
XM_017015611.1:c.933+1251C>G XP_016871100.1:p.=
XM_017015612.1:c.933+1251C>G XP_016871101.1:p.=
XR_001747010.1:n.1011+1251C>G
XR_001747011.1:n.1011+1251C>G
NM_001278.5:c.933+1251C>G VV MANE Preferred
ENST00000370397.7:c.933+1251C>G ENSP00000359424.6:p.=