Canonical Allele Identifier: CA2244611724

Gene: C17orf107 CHRNE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4900751C= , CM000679.2:g.4900751C=	GRCh38
NC_000017.10:g.4804046C= , CM000679.1:g.4804046C=	GRCh37
NC_000017.9:g.4744825C=	NCBI36
NG_008029.2:g.7325G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381365.4:c.*218C= (C17orf107) MANE Select	ENSP00000370770.3:n.*218C=
ENST00000649488.2:c.917+42G= (CHRNE) MANE Select	ENSP00000497829.1:n.917+42G=
ENST00000649830.1:c.-17+42G= (CHRNE)	ENSP00000496907.1:n.-17+42G=
ENST00000293780.4:c.917+42G= (CHRNE)	ENSP00000293780.4:n.917+42G=
ENST00000381365.3:c.*218C= (C17orf107)	ENSP00000370770.3:n.*218C=
ENST00000521575.1:c.*585C= (C17orf107)	ENSP00000429241.1:n.*585C=
ENST00000572438.1:n.603+42G= (CHRNE)
NM_000080.3:c.917+42G= (CHRNE)	NP_000071.1:n.917+42G=
NM_001145536.1:c.*218C= (C17orf107)	NP_001139008.1:n.*218C=
XM_011523612.1:c.546+245C= (C17orf107)	XP_011521914.1:n.546+245C=
XM_011523631.1:c.802+239G= (CHRNE)	XP_011521933.1:n.802+239G=
NM_000080.4:c.917+42G= (CHRNE) MANE Select	NP_000071.1:n.917+42G=
XM_017024115.1:c.881+42G= (CHRNE)	XP_016879604.1:n.881+42G=
XR_001752421.1:n.1647+239G= (CHRNE)
NM_001145536.2:c.*218C= (C17orf107) MANE Select	NP_001139008.1:n.*218C=