Canonical Allele Identifier: CA212896821

Gene: CHUK

Linked Data

• dbSNP Id: rs931813315
• gnomAD v3: 10-100216677-C-T
• gnomAD v4: 10-100216677-C-T
• MyVariant Identifiers: chr10:g.101976434C>T (hg19) ; chr10:g.100216677C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100216677C>T , CM000672.2:g.100216677C>T	GRCh38
NC_000010.10:g.101976434C>T , CM000672.1:g.101976434C>T	GRCh37
NC_000010.9:g.101966424C>T	NCBI36
NG_028023.1:g.17911G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370397.8:c.933+1318G>A MANE Select	ENSP00000359424.6:n.933+1318G>A
ENST00000370397.7:c.933+1318G>A	ENSP00000359424.6:n.933+1318G>A
NM_001278.3:c.933+1318G>A	NP_001269.3:n.933+1318G>A
XM_011539196.1:c.933+1318G>A	XP_011537498.1:n.933+1318G>A
XM_011539197.1:c.933+1318G>A	XP_011537499.1:n.933+1318G>A
XM_011539198.1:c.933+1318G>A	XP_011537500.1:n.933+1318G>A
XR_945589.1:n.1011+1318G>A
XR_945590.1:n.1011+1318G>A
NM_001278.4:c.933+1318G>A	NP_001269.3:n.933+1318G>A
NM_001320928.1:c.933+1318G>A	NP_001307857.1:n.933+1318G>A
XM_017015611.1:c.933+1318G>A	XP_016871100.1:n.933+1318G>A
XM_017015612.1:c.933+1318G>A	XP_016871101.1:n.933+1318G>A
XR_001747010.1:n.1011+1318G>A
XR_001747011.1:n.1011+1318G>A
NM_001278.5:c.933+1318G>A MANE Select	NP_001269.3:n.933+1318G>A
NM_001320928.2:c.933+1318G>A	NP_001307857.1:n.933+1318G>A