Canonical Allele Identifier: CA397307482
Gene: C17orf107 HGNC NCBI
CHRNE HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.4805756A>T (hg19) chr17:g.4902461A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4902461A>T , CM000679.2:g.4902461A>T GRCh38
NC_000017.10:g.4805756A>T , CM000679.1:g.4805756A>T GRCh37
NC_000017.9:g.4746535A>T NCBI36
NG_008029.2:g.5615T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000381365.4:c.*1928A>T (C17orf107) MANE Select ENSP00000370770.3:n.*1928A>T
ENST00000649488.2:c.223T>A (CHRNE) MANE Select ENSP00000497829.1:p.Trp75Arg
ENST00000649830.1:c.-711T>A (CHRNE) ENSP00000496907.1:n.-711T>A
ENST00000293780.4:c.223T>A (CHRNE) ENSP00000293780.4:p.Trp75Arg
ENST00000381365.3:c.*1928A>T (C17orf107) ENSP00000370770.3:n.*1928A>T
ENST00000575637.1:n.44T>A (CHRNE)
NM_000080.3:c.223T>A (CHRNE) NP_000071.1:p.Trp75Arg
NM_001145536.1:c.*1928A>T (C17orf107) NP_001139008.1:n.*1928A>T
XM_011523612.1:c.546+1955A>T (C17orf107) XP_011521914.1:n.546+1955A>T
XM_011523631.1:c.223T>A (CHRNE) XP_011521933.1:p.Trp75Arg
NM_000080.4:c.223T>A (CHRNE) MANE Select NP_000071.1:p.Trp75Arg
XM_017024115.1:c.187T>A (CHRNE) XP_016879604.1:p.Trp63Arg
XR_001752421.1:n.1068T>A (CHRNE)
NM_001145536.2:c.*1928A>T (C17orf107) MANE Select NP_001139008.1:n.*1928A>T
Search 100 bp 5'
Search 100 bp 3'