Canonical Allele Identifier: CA397300900

Gene: CHRNE C17orf107

Linked Data

• dbSNP Id: rs747017964
• MyVariant Identifiers: chr17:g.4802806T>A (hg19) ; chr17:g.4899511T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4899511T>A , CM000679.2:g.4899511T>A	GRCh38
NC_000017.10:g.4802806T>A , CM000679.1:g.4802806T>A	GRCh37
NC_000017.9:g.4743585T>A	NCBI36
NG_008029.2:g.8565A>T
NG_028005.1:g.71172T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649488.2:c.989A>T (CHRNE) MANE Select	ENSP00000497829.1:p.Gln330Leu
ENST00000649830.1:c.56A>T (CHRNE)	ENSP00000496907.1:p.Gln19Leu
ENST00000652550.1:n.719A>T (CHRNE)
ENST00000293780.4:c.989A>T (CHRNE)	ENSP00000293780.4:p.Gln330Leu
ENST00000521575.1:c.-252T>A (C17orf107)	ENSP00000429241.1:n.-252T>A
ENST00000572438.1:n.675A>T (CHRNE)
NM_000080.3:c.989A>T (CHRNE)	NP_000071.1:p.Gln330Leu
XM_011523612.1:c.-252T>A (C17orf107)	XP_011521914.1:n.-252T>A
XM_011523631.1:c.*28A>T (CHRNE)	XP_011521933.1:n.*28A>T
NM_000080.4:c.989A>T (CHRNE) MANE Select	NP_000071.1:p.Gln330Leu
XM_017024115.1:c.953A>T (CHRNE)	XP_016879604.1:p.Gln318Leu
XR_001752421.1:n.1719A>T (CHRNE)