Canonical Allele Identifier: CA497675728

Gene: CHRNE

Linked Data

• MyVariant Identifiers: chr17:g.4802040G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4898745G>T , CM000679.2:g.4898745G>T	GRCh38
NC_000017.10:g.4802040G>T , CM000679.1:g.4802040G>T	GRCh37
NC_000017.9:g.4742819G>T	NCBI36
NG_008029.2:g.9331C>A
NG_028005.1:g.70406G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649488.2:c.1473C>A MANE Select	ENSP00000497829.1:p.Ile491=
ENST00000649830.1:c.*109C>A	ENSP00000496907.1:n.*109C>A
ENST00000652550.1:n.1199C>A
ENST00000293780.4:c.1473C>A	ENSP00000293780.4:p.Ile491=
ENST00000572438.1:n.1159C>A
NM_000080.3:c.1473C>A	NP_000071.1:p.Ile491=
NM_000080.4:c.1473C>A MANE Select	NP_000071.1:p.Ile491=
XM_017024115.1:c.1437C>A	XP_016879604.1:p.Ile479=