Canonical Allele Identifier: CA624856034

Gene: C17orf107 CHRNE

Linked Data

• dbSNP Id: rs1309891561
• gnomAD v2: 17-4805215-A-G
• gnomAD v4: 17-4901920-A-G
• MyVariant Identifiers: chr17:g.4805215A>G (hg19) ; chr17:g.4901920A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4901920A>G , CM000679.2:g.4901920A>G	GRCh38
NC_000017.10:g.4805215A>G , CM000679.1:g.4805215A>G	GRCh37
NC_000017.9:g.4745994A>G	NCBI36
NG_008029.2:g.6156T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381365.4:c.*1387A>G (C17orf107) MANE Select	ENSP00000370770.3:n.*1387A>G
ENST00000649488.2:c.500+12T>C (CHRNE) MANE Select	ENSP00000497829.1:n.500+12T>C
ENST00000649830.1:c.-434+12T>C (CHRNE)	ENSP00000496907.1:n.-434+12T>C
ENST00000293780.4:c.500+12T>C (CHRNE)	ENSP00000293780.4:n.500+12T>C
ENST00000381365.3:c.*1387A>G (C17orf107)	ENSP00000370770.3:n.*1387A>G
ENST00000575637.1:n.274+59T>C (CHRNE)
NM_000080.3:c.500+12T>C (CHRNE)	NP_000071.1:n.500+12T>C
NM_001145536.1:c.*1387A>G (C17orf107)	NP_001139008.1:n.*1387A>G
XM_011523612.1:c.546+1414A>G (C17orf107)	XP_011521914.1:n.546+1414A>G
XM_011523631.1:c.500+12T>C (CHRNE)	XP_011521933.1:n.500+12T>C
NM_000080.4:c.500+12T>C (CHRNE) MANE Select	NP_000071.1:n.500+12T>C
XM_017024115.1:c.464+12T>C (CHRNE)	XP_016879604.1:n.464+12T>C
XR_001752421.1:n.1345+12T>C (CHRNE)
NM_001145536.2:c.*1387A>G (C17orf107) MANE Select	NP_001139008.1:n.*1387A>G