Canonical Allele Identifier: CA2244611769

Gene: C17orf107 CHRNE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4900805G= , CM000679.2:g.4900805G=	GRCh38
NC_000017.10:g.4804100G= , CM000679.1:g.4804100G=	GRCh37
NC_000017.9:g.4744879G=	NCBI36
NG_008029.2:g.7271C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000080.4:c.905C= (CHRNE) MANE Select	NP_000071.1:p.Pro302=
NM_001145536.2:c.*272G= (C17orf107) MANE Select	NP_001139008.1:n.*272G=
ENST00000381365.4:c.*272G= (C17orf107) MANE Select	ENSP00000370770.3:n.*272G=
ENST00000649488.2:c.905C= (CHRNE) MANE Select	ENSP00000497829.1:p.Pro302=
NM_000080.3:c.905C= (CHRNE)	NP_000071.1:p.Pro302=
NM_001145536.1:c.*272G= (C17orf107)	NP_001139008.1:n.*272G=
ENST00000293780.4:c.905C= (CHRNE)	ENSP00000293780.4:p.Pro302=
ENST00000381365.3:c.*272G= (C17orf107)	ENSP00000370770.3:n.*272G=
ENST00000572438.1:n.591C= (CHRNE)
ENST00000649830.1:c.-29C= (CHRNE)	ENSP00000496907.1:n.-29C=
XM_011523612.1:c.546+299G= (C17orf107)	XP_011521914.1:n.546+299G=
XM_011523631.1:c.802+185C= (CHRNE)	XP_011521933.1:n.802+185C=
XM_017024115.1:c.869C= (CHRNE)	XP_016879604.1:p.Pro290=
XR_001752421.1:n.1647+185C= (CHRNE)