Canonical Allele Identifier: CA2244612699
Gene: C17orf107 HGNC NCBI
CHRNE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4902173C= , CM000679.2:g.4902173C= GRCh38
NC_000017.10:g.4805468C= , CM000679.1:g.4805468C= GRCh37
NC_000017.9:g.4746247C= NCBI36
NG_008029.2:g.5903G=

Transcript Alleles

HGVS Amino-acid change
ENST00000381365.4:c.*1640C= (C17orf107) MANE Select ENSP00000370770.3:n.*1640C=
ENST00000649488.2:c.344+44G= (CHRNE) MANE Select ENSP00000497829.1:n.344+44G=
ENST00000649830.1:c.-590+44G= (CHRNE) ENSP00000496907.1:n.-590+44G=
ENST00000293780.4:c.344+44G= (CHRNE) ENSP00000293780.4:n.344+44G=
ENST00000381365.3:c.*1640C= (C17orf107) ENSP00000370770.3:n.*1640C=
ENST00000575637.1:n.165+44G= (CHRNE)
NM_000080.3:c.344+44G= (CHRNE) NP_000071.1:n.344+44G=
NM_001145536.1:c.*1640C= (C17orf107) NP_001139008.1:n.*1640C=
XM_011523612.1:c.546+1667C= (C17orf107) XP_011521914.1:n.546+1667C=
XM_011523631.1:c.344+44G= (CHRNE) XP_011521933.1:n.344+44G=
NM_000080.4:c.344+44G= (CHRNE) MANE Select NP_000071.1:n.344+44G=
XM_017024115.1:c.308+44G= (CHRNE) XP_016879604.1:n.308+44G=
XR_001752421.1:n.1189+44G= (CHRNE)
NM_001145536.2:c.*1640C= (C17orf107) MANE Select NP_001139008.1:n.*1640C=