Canonical Allele Identifier: CA2244612618

Gene: C17orf107 CHRNE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4902055G= , CM000679.2:g.4902055G=	GRCh38
NC_000017.10:g.4805350G= , CM000679.1:g.4805350G=	GRCh37
NC_000017.9:g.4746129G=	NCBI36
NG_008029.2:g.6021C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381365.4:c.*1522G= (C17orf107) MANE Select	ENSP00000370770.3:n.*1522G=
ENST00000649488.2:c.377C= (CHRNE) MANE Select	ENSP00000497829.1:p.Ala126=
ENST00000649830.1:c.-557C= (CHRNE)	ENSP00000496907.1:n.-557C=
ENST00000293780.4:c.377C= (CHRNE)	ENSP00000293780.4:p.Ala126=
ENST00000381365.3:c.*1522G= (C17orf107)	ENSP00000370770.3:n.*1522G=
ENST00000575637.1:n.198C= (CHRNE)
NM_000080.3:c.377C= (CHRNE)	NP_000071.1:p.Ala126=
NM_001145536.1:c.*1522G= (C17orf107)	NP_001139008.1:n.*1522G=
XM_011523612.1:c.546+1549G= (C17orf107)	XP_011521914.1:n.546+1549G=
XM_011523631.1:c.377C= (CHRNE)	XP_011521933.1:p.Ala126=
NM_000080.4:c.377C= (CHRNE) MANE Select	NP_000071.1:p.Ala126=
XM_017024115.1:c.341C= (CHRNE)	XP_016879604.1:p.Ala114=
XR_001752421.1:n.1222C= (CHRNE)
NM_001145536.2:c.*1522G= (C17orf107) MANE Select	NP_001139008.1:n.*1522G=