Canonical Allele Identifier: CA2244612757

Gene: C17orf107 CHRNE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4902298C= , CM000679.2:g.4902298C=	GRCh38
NC_000017.10:g.4805593C= , CM000679.1:g.4805593C=	GRCh37
NC_000017.9:g.4746372C=	NCBI36
NG_008029.2:g.5778G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381365.4:c.*1765C= (C17orf107) MANE Select	ENSP00000370770.3:n.*1765C=
ENST00000649488.2:c.263G= (CHRNE) MANE Select	ENSP00000497829.1:p.Ser88=
ENST00000649830.1:c.-671G= (CHRNE)	ENSP00000496907.1:n.-671G=
ENST00000293780.4:c.263G= (CHRNE)	ENSP00000293780.4:p.Ser88=
ENST00000381365.3:c.*1765C= (C17orf107)	ENSP00000370770.3:n.*1765C=
ENST00000575637.1:n.84G= (CHRNE)
NM_000080.3:c.263G= (CHRNE)	NP_000071.1:p.Ser88=
NM_001145536.1:c.*1765C= (C17orf107)	NP_001139008.1:n.*1765C=
XM_011523612.1:c.546+1792C= (C17orf107)	XP_011521914.1:n.546+1792C=
XM_011523631.1:c.263G= (CHRNE)	XP_011521933.1:p.Ser88=
NM_000080.4:c.263G= (CHRNE) MANE Select	NP_000071.1:p.Ser88=
XM_017024115.1:c.227G= (CHRNE)	XP_016879604.1:p.Ser76=
XR_001752421.1:n.1108G= (CHRNE)
NM_001145536.2:c.*1765C= (C17orf107) MANE Select	NP_001139008.1:n.*1765C=