Canonical Allele Identifier: CA378147975

Gene: CHUK

Linked Data

• MyVariant Identifiers: chr10:g.101953802G>T (hg19) ; chr10:g.100194045G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100194045G>T , CM000672.2:g.100194045G>T	GRCh38
NC_000010.10:g.101953802G>T , CM000672.1:g.101953802G>T	GRCh37
NC_000010.9:g.101943792G>T	NCBI36
NG_028023.1:g.40543C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370397.8:c.1913C>A MANE Select	ENSP00000359424.6:p.Thr638Asn
ENST00000370397.7:c.1913C>A	ENSP00000359424.6:p.Thr638Asn
ENST00000588656.1:n.35C>A
ENST00000590930.5:n.1898C>A
NM_001278.3:c.1913C>A	NP_001269.3:p.Thr638Asn
XM_011539196.1:c.1913C>A	XP_011537498.1:p.Thr638Asn
XM_011539197.1:c.1913C>A	XP_011537499.1:p.Thr638Asn
XM_011539198.1:c.1913C>A	XP_011537500.1:p.Thr638Asn
XR_945589.1:n.1991C>A
NM_001278.4:c.1913C>A	NP_001269.3:p.Thr638Asn
NM_001320928.1:c.1913C>A	NP_001307857.1:p.Thr638Asn
XM_017015611.1:c.1913C>A	XP_016871100.1:p.Thr638Asn
XM_017015613.1:c.701C>A	XP_016871102.1:p.Thr234Asn
XR_001747010.1:n.1991C>A
XR_001747011.1:n.1888C>A
NM_001278.5:c.1913C>A MANE Select	NP_001269.3:p.Thr638Asn
NM_001320928.2:c.1913C>A	NP_001307857.1:p.Thr638Asn