Canonical Allele Identifier: CA497675950

Gene: CHRNE C17orf107

Linked Data

• MyVariant Identifiers: chr17:g.4802769C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4899474C>G , CM000679.2:g.4899474C>G	GRCh38
NC_000017.10:g.4802769C>G , CM000679.1:g.4802769C>G	GRCh37
NC_000017.9:g.4743548C>G	NCBI36
NG_008029.2:g.8602G>C
NG_028005.1:g.71135C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649488.2:c.1026G>C (CHRNE) MANE Select	ENSP00000497829.1:p.Leu342=
ENST00000649830.1:c.93G>C (CHRNE)	ENSP00000496907.1:p.Leu31=
ENST00000652550.1:n.756G>C (CHRNE)
ENST00000293780.4:c.1026G>C (CHRNE)	ENSP00000293780.4:p.Leu342=
ENST00000521575.1:c.-289C>G (C17orf107)	ENSP00000429241.1:n.-289C>G
ENST00000572438.1:n.712G>C (CHRNE)
NM_000080.3:c.1026G>C (CHRNE)	NP_000071.1:p.Leu342=
XM_011523612.1:c.-289C>G (C17orf107)	XP_011521914.1:n.-289C>G
NM_000080.4:c.1026G>C (CHRNE) MANE Select	NP_000071.1:p.Leu342=
XM_017024115.1:c.990G>C (CHRNE)	XP_016879604.1:p.Leu330=
XR_001752421.1:n.1756G>C (CHRNE)