Canonical Allele Identifier: CA2244610331

Gene: CHRNE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4898768C= , CM000679.2:g.4898768C=	GRCh38
NC_000017.10:g.4802063C= , CM000679.1:g.4802063C=	GRCh37
NC_000017.9:g.4742842C=	NCBI36
NG_008029.2:g.9308G=
NG_028005.1:g.70429C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649488.2:c.1450G= MANE Select	ENSP00000497829.1:p.Asp484=
ENST00000649830.1:c.*86G=	ENSP00000496907.1:n.*86G=
ENST00000652550.1:n.1176G=
ENST00000293780.4:c.1450G=	ENSP00000293780.4:p.Asp484=
ENST00000572438.1:n.1136G=
NM_000080.3:c.1450G=	NP_000071.1:p.Asp484=
NM_000080.4:c.1450G= MANE Select	NP_000071.1:p.Asp484=
XM_017024115.1:c.1414G=	XP_016879604.1:p.Asp472=