Canonical Allele Identifier: CA2244610927

Gene: CHRNE C17orf107

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4899492G= , CM000679.2:g.4899492G=	GRCh38
NC_000017.10:g.4802787G= , CM000679.1:g.4802787G=	GRCh37
NC_000017.9:g.4743566G=	NCBI36
NG_008029.2:g.8584C=
NG_028005.1:g.71153G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649488.2:c.1008C= (CHRNE) MANE Select	ENSP00000497829.1:p.His336=
ENST00000649830.1:c.75C= (CHRNE)	ENSP00000496907.1:p.His25=
ENST00000652550.1:n.738C= (CHRNE)
ENST00000293780.4:c.1008C= (CHRNE)	ENSP00000293780.4:p.His336=
ENST00000521575.1:c.-271G= (C17orf107)	ENSP00000429241.1:n.-271G=
ENST00000572438.1:n.694C= (CHRNE)
NM_000080.3:c.1008C= (CHRNE)	NP_000071.1:p.His336=
XM_011523612.1:c.-271G= (C17orf107)	XP_011521914.1:n.-271G=
NM_000080.4:c.1008C= (CHRNE) MANE Select	NP_000071.1:p.His336=
XM_017024115.1:c.972C= (CHRNE)	XP_016879604.1:p.His324=
XR_001752421.1:n.1738C= (CHRNE)