Canonical Allele Identifier: CA2244610980

Gene: C17orf107 CHRNE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4899563C= , CM000679.2:g.4899563C=	GRCh38
NC_000017.10:g.4802858C= , CM000679.1:g.4802858C=	GRCh37
NC_000017.9:g.4743637C=	NCBI36
NG_008029.2:g.8513G=
NG_028005.1:g.71224C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381365.4:c.-200C= (C17orf107) MANE Select	ENSP00000370770.3:n.-200C=
ENST00000649488.2:c.937G= (CHRNE) MANE Select	ENSP00000497829.1:p.Val313=
ENST00000649830.1:c.4G= (CHRNE)	ENSP00000496907.1:p.Val2=
ENST00000652550.1:n.667G= (CHRNE)
ENST00000293780.4:c.937G= (CHRNE)	ENSP00000293780.4:p.Val313=
ENST00000381365.3:c.-200C= (C17orf107)	ENSP00000370770.3:n.-200C=
ENST00000521575.1:c.-200C= (C17orf107)	ENSP00000429241.1:n.-200C=
ENST00000572438.1:n.623G= (CHRNE)
NM_000080.3:c.937G= (CHRNE)	NP_000071.1:p.Val313=
XM_011523612.1:c.-200C= (C17orf107)	XP_011521914.1:n.-200C=
XM_011523631.1:c.822G= (CHRNE)	XP_011521933.1:p.Trp274=
NM_000080.4:c.937G= (CHRNE) MANE Select	NP_000071.1:p.Val313=
XM_017024115.1:c.901G= (CHRNE)	XP_016879604.1:p.Val301=
XR_001752421.1:n.1667G= (CHRNE)
NM_001145536.2:c.-200C= (C17orf107) MANE Select	NP_001139008.1:n.-200C=