Canonical Allele Identifier: CA10575540

Gene: C17orf107 CHRNE

Linked Data

• ClinVar Variation Id: 18362
• ClinVar RCV Id: RCV000020030 ; RCV003466866
• dbSNP Id: rs879255563
• MyVariant Identifiers: chr17:g.4804936C>T (hg19) ; chr17:g.4901641C>T (hg38)
• PubMed: PMID:16087917

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4901641C>T , CM000679.2:g.4901641C>T	GRCh38
NC_000017.10:g.4804936C>T , CM000679.1:g.4804936C>T	GRCh37
NC_000017.9:g.4745715C>T	NCBI36
NG_008029.2:g.6435G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381365.4:c.*1108C>T (C17orf107) MANE Select	ENSP00000370770.3:n.*1108C>T
ENST00000649488.2:c.501-16G>A (CHRNE) MANE Select	ENSP00000497829.1:n.501-16G>A
ENST00000649830.1:c.-433-16G>A (CHRNE)	ENSP00000496907.1:n.-433-16G>A
ENST00000293780.4:c.501-16G>A (CHRNE)	ENSP00000293780.4:n.501-16G>A
ENST00000381365.3:c.*1108C>T (C17orf107)	ENSP00000370770.3:n.*1108C>T
ENST00000572438.1:n.171G>A (CHRNE)
ENST00000575637.1:n.275-16G>A (CHRNE)
NM_000080.3:c.501-16G>A (CHRNE)	NP_000071.1:n.501-16G>A
NM_001145536.1:c.*1108C>T (C17orf107)	NP_001139008.1:n.*1108C>T
XM_011523612.1:c.546+1135C>T (C17orf107)	XP_011521914.1:n.546+1135C>T
XM_011523631.1:c.501-16G>A (CHRNE)	XP_011521933.1:n.501-16G>A
NM_000080.4:c.501-16G>A (CHRNE) MANE Select	NP_000071.1:n.501-16G>A
XM_017024115.1:c.465-16G>A (CHRNE)	XP_016879604.1:n.465-16G>A
XR_001752421.1:n.1346-16G>A (CHRNE)
NM_001145536.2:c.*1108C>T (C17orf107) MANE Select	NP_001139008.1:n.*1108C>T