Canonical Allele Identifier: CA2244610349

Gene: CHRNE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4898799G= , CM000679.2:g.4898799G=	GRCh38
NC_000017.10:g.4802094G= , CM000679.1:g.4802094G=	GRCh37
NC_000017.9:g.4742873G=	NCBI36
NG_008029.2:g.9277C=
NG_028005.1:g.70460G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649488.2:c.1419C= MANE Select	ENSP00000497829.1:p.Ile473=
ENST00000649830.1:c.*55C=	ENSP00000496907.1:n.*55C=
ENST00000652550.1:n.1145C=
ENST00000293780.4:c.1419C=	ENSP00000293780.4:p.Ile473=
ENST00000572438.1:n.1105C=
NM_000080.3:c.1419C=	NP_000071.1:p.Ile473=
NM_000080.4:c.1419C= MANE Select	NP_000071.1:p.Ile473=
XM_017024115.1:c.1383C=	XP_016879604.1:p.Ile461=