Canonical Allele Identifier: CA2244612604

Gene: C17orf107 CHRNE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4902032C= , CM000679.2:g.4902032C=	GRCh38
NC_000017.10:g.4805327C= , CM000679.1:g.4805327C=	GRCh37
NC_000017.9:g.4746106C=	NCBI36
NG_008029.2:g.6044G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381365.4:c.*1499C= (C17orf107) MANE Select	ENSP00000370770.3:n.*1499C=
ENST00000649488.2:c.400G= (CHRNE) MANE Select	ENSP00000497829.1:p.Gly134=
ENST00000649830.1:c.-534G= (CHRNE)	ENSP00000496907.1:n.-534G=
ENST00000293780.4:c.400G= (CHRNE)	ENSP00000293780.4:p.Gly134=
ENST00000381365.3:c.*1499C= (C17orf107)	ENSP00000370770.3:n.*1499C=
ENST00000575637.1:n.221G= (CHRNE)
NM_000080.3:c.400G= (CHRNE)	NP_000071.1:p.Gly134=
NM_001145536.1:c.*1499C= (C17orf107)	NP_001139008.1:n.*1499C=
XM_011523612.1:c.546+1526C= (C17orf107)	XP_011521914.1:n.546+1526C=
XM_011523631.1:c.400G= (CHRNE)	XP_011521933.1:p.Gly134=
NM_000080.4:c.400G= (CHRNE) MANE Select	NP_000071.1:p.Gly134=
XM_017024115.1:c.364G= (CHRNE)	XP_016879604.1:p.Gly122=
XR_001752421.1:n.1245G= (CHRNE)
NM_001145536.2:c.*1499C= (C17orf107) MANE Select	NP_001139008.1:n.*1499C=