Canonical Allele Identifier: CA2244610877

Gene: CHRNE C17orf107

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4899430C= , CM000679.2:g.4899430C=	GRCh38
NC_000017.10:g.4802725C= , CM000679.1:g.4802725C=	GRCh37
NC_000017.9:g.4743504C=	NCBI36
NG_008029.2:g.8646G=
NG_028005.1:g.71091C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000649488.2:c.1032+38G= (CHRNE) MANE Select	ENSP00000497829.1:n.1032+38G=
ENST00000649830.1:c.99+38G= (CHRNE)	ENSP00000496907.1:n.99+38G=
ENST00000652550.1:n.762+38G= (CHRNE)
ENST00000293780.4:c.1032+38G= (CHRNE)	ENSP00000293780.4:n.1032+38G=
ENST00000521575.1:c.-333C= (C17orf107)	ENSP00000429241.1:n.-333C=
ENST00000572438.1:n.718+38G= (CHRNE)
NM_000080.3:c.1032+38G= (CHRNE)	NP_000071.1:n.1032+38G=
NM_000080.4:c.1032+38G= (CHRNE) MANE Select	NP_000071.1:n.1032+38G=
XM_017024115.1:c.996+38G= (CHRNE)	XP_016879604.1:n.996+38G=
XR_001752421.1:n.1762+38G= (CHRNE)