Canonical Allele Identifier: CA397307169
Gene: C17orf107 HGNC NCBI
CHRNE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4902286A>C , CM000679.2:g.4902286A>C GRCh38
NC_000017.10:g.4805581A>C , CM000679.1:g.4805581A>C GRCh37
NC_000017.9:g.4746360A>C NCBI36
NG_008029.2:g.5790T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381365.4:c.*1753A>C (C17orf107) MANE Select ENSP00000370770.3:n.*1753A>C
ENST00000649488.2:c.275T>G (CHRNE) MANE Select ENSP00000497829.1:p.Phe92Cys
ENST00000649830.1:c.-659T>G (CHRNE) ENSP00000496907.1:n.-659T>G
ENST00000293780.4:c.275T>G (CHRNE) ENSP00000293780.4:p.Phe92Cys
ENST00000381365.3:c.*1753A>C (C17orf107) ENSP00000370770.3:n.*1753A>C
ENST00000575637.1:n.96T>G (CHRNE)
NM_000080.3:c.275T>G (CHRNE) NP_000071.1:p.Phe92Cys
NM_001145536.1:c.*1753A>C (C17orf107) NP_001139008.1:n.*1753A>C
XM_011523612.1:c.546+1780A>C (C17orf107) XP_011521914.1:n.546+1780A>C
XM_011523631.1:c.275T>G (CHRNE) XP_011521933.1:p.Phe92Cys
NM_000080.4:c.275T>G (CHRNE) MANE Select NP_000071.1:p.Phe92Cys
XM_017024115.1:c.239T>G (CHRNE) XP_016879604.1:p.Phe80Cys
XR_001752421.1:n.1120T>G (CHRNE)
NM_001145536.2:c.*1753A>C (C17orf107) MANE Select NP_001139008.1:n.*1753A>C