Canonical Allele Identifier: CA2244611950

Gene: C17orf107 CHRNE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4901071G= , CM000679.2:g.4901071G=	GRCh38
NC_000017.10:g.4804366G= , CM000679.1:g.4804366G=	GRCh37
NC_000017.9:g.4745145G=	NCBI36
NG_008029.2:g.7005C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000080.4:c.721C= (CHRNE) MANE Select	NP_000071.1:p.Leu241=
NM_001145536.2:c.*538G= (C17orf107) MANE Select	NP_001139008.1:n.*538G=
ENST00000381365.4:c.*538G= (C17orf107) MANE Select	ENSP00000370770.3:n.*538G=
ENST00000649488.2:c.721C= (CHRNE) MANE Select	ENSP00000497829.1:p.Leu241=
NM_000080.3:c.721C= (CHRNE)	NP_000071.1:p.Leu241=
NM_001145536.1:c.*538G= (C17orf107)	NP_001139008.1:n.*538G=
ENST00000293780.4:c.721C= (CHRNE)	ENSP00000293780.4:p.Leu241=
ENST00000381365.3:c.*538G= (C17orf107)	ENSP00000370770.3:n.*538G=
ENST00000572438.1:n.407C= (CHRNE)
ENST00000575637.1:n.495C= (CHRNE)
ENST00000649830.1:c.-213C= (CHRNE)	ENSP00000496907.1:n.-213C=
XM_011523612.1:c.546+565G= (C17orf107)	XP_011521914.1:n.546+565G=
XM_011523631.1:c.721C= (CHRNE)	XP_011521933.1:p.Leu241=
XM_017024115.1:c.685C= (CHRNE)	XP_016879604.1:p.Leu229=
XR_001752421.1:n.1566C= (CHRNE)