Canonical Allele Identifier: CA497676015

Gene: CHRNE C17orf107

Linked Data

• gnomAD v4: 17-4899510-C-T
• MyVariant Identifiers: chr17:g.4802805C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4899510C>T , CM000679.2:g.4899510C>T	GRCh38
NC_000017.10:g.4802805C>T , CM000679.1:g.4802805C>T	GRCh37
NC_000017.9:g.4743584C>T	NCBI36
NG_008029.2:g.8566G>A
NG_028005.1:g.71171C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649488.2:c.990G>A (CHRNE) MANE Select	ENSP00000497829.1:p.Gln330=
ENST00000649830.1:c.57G>A (CHRNE)	ENSP00000496907.1:p.Gln19=
ENST00000652550.1:n.720G>A (CHRNE)
ENST00000293780.4:c.990G>A (CHRNE)	ENSP00000293780.4:p.Gln330=
ENST00000521575.1:c.-253C>T (C17orf107)	ENSP00000429241.1:n.-253C>T
ENST00000572438.1:n.676G>A (CHRNE)
NM_000080.3:c.990G>A (CHRNE)	NP_000071.1:p.Gln330=
XM_011523612.1:c.-253C>T (C17orf107)	XP_011521914.1:n.-253C>T
XM_011523631.1:c.*29G>A (CHRNE)	XP_011521933.1:n.*29G>A
NM_000080.4:c.990G>A (CHRNE) MANE Select	NP_000071.1:p.Gln330=
XM_017024115.1:c.954G>A (CHRNE)	XP_016879604.1:p.Gln318=
XR_001752421.1:n.1720G>A (CHRNE)