Canonical Allele Identifier: CA2244610332

Gene: CHRNE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4898771G= , CM000679.2:g.4898771G=	GRCh38
NC_000017.10:g.4802066G= , CM000679.1:g.4802066G=	GRCh37
NC_000017.9:g.4742845G=	NCBI36
NG_008029.2:g.9305C=
NG_028005.1:g.70432G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649488.2:c.1447C= MANE Select	ENSP00000497829.1:p.Pro483=
ENST00000649830.1:c.*83C=	ENSP00000496907.1:n.*83C=
ENST00000652550.1:n.1173C=
ENST00000293780.4:c.1447C=	ENSP00000293780.4:p.Pro483=
ENST00000572438.1:n.1133C=
NM_000080.3:c.1447C=	NP_000071.1:p.Pro483=
NM_000080.4:c.1447C= MANE Select	NP_000071.1:p.Pro483=
XM_017024115.1:c.1411C=	XP_016879604.1:p.Pro471=