Canonical Allele Identifier: CA2244611910

Gene: C17orf107 CHRNE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4900998G= , CM000679.2:g.4900998G=	GRCh38
NC_000017.10:g.4804293G= , CM000679.1:g.4804293G=	GRCh37
NC_000017.9:g.4745072G=	NCBI36
NG_008029.2:g.7078C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000080.4:c.794C= (CHRNE) MANE Select	NP_000071.1:p.Pro265=
NM_001145536.2:c.*465G= (C17orf107) MANE Select	NP_001139008.1:n.*465G=
ENST00000381365.4:c.*465G= (C17orf107) MANE Select	ENSP00000370770.3:n.*465G=
ENST00000649488.2:c.794C= (CHRNE) MANE Select	ENSP00000497829.1:p.Pro265=
NM_000080.3:c.794C= (CHRNE)	NP_000071.1:p.Pro265=
NM_001145536.1:c.*465G= (C17orf107)	NP_001139008.1:n.*465G=
ENST00000293780.4:c.794C= (CHRNE)	ENSP00000293780.4:p.Pro265=
ENST00000381365.3:c.*465G= (C17orf107)	ENSP00000370770.3:n.*465G=
ENST00000572438.1:n.480C= (CHRNE)
ENST00000649830.1:c.-140C= (CHRNE)	ENSP00000496907.1:n.-140C=
XM_011523612.1:c.546+492G= (C17orf107)	XP_011521914.1:n.546+492G=
XM_011523631.1:c.794C= (CHRNE)	XP_011521933.1:p.Pro265=
XM_017024115.1:c.758C= (CHRNE)	XP_016879604.1:p.Pro253=
XR_001752421.1:n.1639C= (CHRNE)