Canonical Allele Identifier: CA658874830

Gene: CHUK

Linked Data

• dbSNP Id: rs946765343
• MyVariant Identifiers: chr10:g.101976541G>C (hg19) ; chr10:g.100216784G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100216784G>C , CM000672.2:g.100216784G>C	GRCh38
NC_000010.10:g.101976541G>C , CM000672.1:g.101976541G>C	GRCh37
NC_000010.9:g.101966531G>C	NCBI36
NG_028023.1:g.17804C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370397.8:c.933+1211C>G MANE Select	ENSP00000359424.6:n.933+1211C>G
ENST00000370397.7:c.933+1211C>G	ENSP00000359424.6:n.933+1211C>G
NM_001278.3:c.933+1211C>G	NP_001269.3:n.933+1211C>G
XM_011539196.1:c.933+1211C>G	XP_011537498.1:n.933+1211C>G
XM_011539197.1:c.933+1211C>G	XP_011537499.1:n.933+1211C>G
XM_011539198.1:c.933+1211C>G	XP_011537500.1:n.933+1211C>G
XR_945589.1:n.1011+1211C>G
XR_945590.1:n.1011+1211C>G
NM_001278.4:c.933+1211C>G	NP_001269.3:n.933+1211C>G
NM_001320928.1:c.933+1211C>G	NP_001307857.1:n.933+1211C>G
XM_017015611.1:c.933+1211C>G	XP_016871100.1:n.933+1211C>G
XM_017015612.1:c.933+1211C>G	XP_016871101.1:n.933+1211C>G
XR_001747010.1:n.1011+1211C>G
XR_001747011.1:n.1011+1211C>G
NM_001278.5:c.933+1211C>G MANE Select	NP_001269.3:n.933+1211C>G
NM_001320928.2:c.933+1211C>G	NP_001307857.1:n.933+1211C>G