Canonical Allele Identifier: CA2244612738

Gene: C17orf107 CHRNE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4902252T= , CM000679.2:g.4902252T=	GRCh38
NC_000017.10:g.4805547T= , CM000679.1:g.4805547T=	GRCh37
NC_000017.9:g.4746326T=	NCBI36
NG_008029.2:g.5824A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381365.4:c.*1719T= (C17orf107) MANE Select	ENSP00000370770.3:n.*1719T=
ENST00000649488.2:c.309A= (CHRNE) MANE Select	ENSP00000497829.1:p.Glu103=
ENST00000649830.1:c.-625A= (CHRNE)	ENSP00000496907.1:n.-625A=
ENST00000293780.4:c.309A= (CHRNE)	ENSP00000293780.4:p.Glu103=
ENST00000381365.3:c.*1719T= (C17orf107)	ENSP00000370770.3:n.*1719T=
ENST00000575637.1:n.130A= (CHRNE)
NM_000080.3:c.309A= (CHRNE)	NP_000071.1:p.Glu103=
NM_001145536.1:c.*1719T= (C17orf107)	NP_001139008.1:n.*1719T=
XM_011523612.1:c.546+1746T= (C17orf107)	XP_011521914.1:n.546+1746T=
XM_011523631.1:c.309A= (CHRNE)	XP_011521933.1:p.Glu103=
NM_000080.4:c.309A= (CHRNE) MANE Select	NP_000071.1:p.Glu103=
XM_017024115.1:c.273A= (CHRNE)	XP_016879604.1:p.Glu91=
XR_001752421.1:n.1154A= (CHRNE)
NM_001145536.2:c.*1719T= (C17orf107) MANE Select	NP_001139008.1:n.*1719T=