Canonical Allele Identifier: CA2244611792

Gene: C17orf107 CHRNE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4900845G= , CM000679.2:g.4900845G=	GRCh38
NC_000017.10:g.4804140G= , CM000679.1:g.4804140G=	GRCh37
NC_000017.9:g.4744919G=	NCBI36
NG_008029.2:g.7231C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381365.4:c.*312G= (C17orf107) MANE Select	ENSP00000370770.3:n.*312G=
ENST00000649488.2:c.865C= (CHRNE) MANE Select	ENSP00000497829.1:p.Leu289=
ENST00000649830.1:c.-69C= (CHRNE)	ENSP00000496907.1:n.-69C=
ENST00000293780.4:c.865C= (CHRNE)	ENSP00000293780.4:p.Leu289=
ENST00000381365.3:c.*312G= (C17orf107)	ENSP00000370770.3:n.*312G=
ENST00000572438.1:n.551C= (CHRNE)
NM_000080.3:c.865C= (CHRNE)	NP_000071.1:p.Leu289=
NM_001145536.1:c.*312G= (C17orf107)	NP_001139008.1:n.*312G=
XM_011523612.1:c.546+339G= (C17orf107)	XP_011521914.1:n.546+339G=
XM_011523631.1:c.802+145C= (CHRNE)	XP_011521933.1:n.802+145C=
NM_000080.4:c.865C= (CHRNE) MANE Select	NP_000071.1:p.Leu289=
XM_017024115.1:c.829C= (CHRNE)	XP_016879604.1:p.Leu277=
XR_001752421.1:n.1647+145C= (CHRNE)
NM_001145536.2:c.*312G= (C17orf107) MANE Select	NP_001139008.1:n.*312G=