Canonical Allele Identifier: CA2244611808

Gene: C17orf107 CHRNE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4900860T= , CM000679.2:g.4900860T=	GRCh38
NC_000017.10:g.4804155T= , CM000679.1:g.4804155T=	GRCh37
NC_000017.9:g.4744934T=	NCBI36
NG_008029.2:g.7216A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000080.4:c.850A= (CHRNE) MANE Select	NP_000071.1:p.Thr284=
NM_001145536.2:c.*327T= (C17orf107) MANE Select	NP_001139008.1:n.*327T=
ENST00000381365.4:c.*327T= (C17orf107) MANE Select	ENSP00000370770.3:n.*327T=
ENST00000649488.2:c.850A= (CHRNE) MANE Select	ENSP00000497829.1:p.Thr284=
NM_000080.3:c.850A= (CHRNE)	NP_000071.1:p.Thr284=
NM_001145536.1:c.*327T= (C17orf107)	NP_001139008.1:n.*327T=
ENST00000293780.4:c.850A= (CHRNE)	ENSP00000293780.4:p.Thr284=
ENST00000381365.3:c.*327T= (C17orf107)	ENSP00000370770.3:n.*327T=
ENST00000572438.1:n.536A= (CHRNE)
ENST00000649830.1:c.-84A= (CHRNE)	ENSP00000496907.1:n.-84A=
XM_011523612.1:c.546+354T= (C17orf107)	XP_011521914.1:n.546+354T=
XM_011523631.1:c.802+130A= (CHRNE)	XP_011521933.1:n.802+130A=
XM_017024115.1:c.814A= (CHRNE)	XP_016879604.1:p.Thr272=
XR_001752421.1:n.1647+130A= (CHRNE)