Canonical Allele Identifier: CA2244610915
Gene: CHRNE HGNC NCBI
C17orf107 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4899477C= , CM000679.2:g.4899477C= GRCh38
NC_000017.10:g.4802772C= , CM000679.1:g.4802772C= GRCh37
NC_000017.9:g.4743551C= NCBI36
NG_008029.2:g.8599G=
NG_028005.1:g.71138C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.1023G= (CHRNE) MANE Select ENSP00000497829.1:p.Arg341=
ENST00000649830.1:c.90G= (CHRNE) ENSP00000496907.1:p.Arg30=
ENST00000652550.1:n.753G= (CHRNE)
ENST00000293780.4:c.1023G= (CHRNE) ENSP00000293780.4:p.Arg341=
ENST00000521575.1:c.-286C= (C17orf107) ENSP00000429241.1:n.-286C=
ENST00000572438.1:n.709G= (CHRNE)
NM_000080.3:c.1023G= (CHRNE) NP_000071.1:p.Arg341=
XM_011523612.1:c.-286C= (C17orf107) XP_011521914.1:n.-286C=
NM_000080.4:c.1023G= (CHRNE) MANE Select NP_000071.1:p.Arg341=
XM_017024115.1:c.987G= (CHRNE) XP_016879604.1:p.Arg329=
XR_001752421.1:n.1753G= (CHRNE)