Canonical Allele Identifier: CA2244610912
Gene: CHRNE HGNC NCBI
C17orf107 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4899474_4899493delinsCAGCCGCGGGGACATGGCGT , CM000679.2:g.4899474_4899493delinsCAGCCGCGGGGACATGGCGT GRCh38
NC_000017.10:g.4802769_4802788delinsCAGCCGCGGGGACATGGCGT , CM000679.1:g.4802769_4802788delinsCAGCCGCGGGGACATGGCGT GRCh37
NC_000017.9:g.4743548_4743567delinsCAGCCGCGGGGACATGGCGT NCBI36
NG_008029.2:g.8583_8602delinsACGCCATGTCCCCGCGGCTG
NG_028005.1:g.71135_71154delinsCAGCCGCGGGGACATGGCGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.1007_1026delinsACGCCATGTCCCCGCGGCTG (CHRNE) MANE Select ENSP00000497829.1:p.His336=
ENST00000649830.1:c.74_93delinsACGCCATGTCCCCGCGGCTG (CHRNE) ENSP00000496907.1:p.His25=
ENST00000652550.1:n.737_756delinsACGCCATGTCCCCGCGGCTG (CHRNE)
ENST00000293780.4:c.1007_1026delinsACGCCATGTCCCCGCGGCTG (CHRNE) ENSP00000293780.4:p.His336=
ENST00000521575.1:c.-289_-270delinsCAGCCGCGGGGACATGGCGT (C17orf107) ENSP00000429241.1:n.-289_-270delinsCAGCCGCGGGGACATGGCGT
ENST00000572438.1:n.693_712delinsACGCCATGTCCCCGCGGCTG (CHRNE)
NM_000080.3:c.1007_1026delinsACGCCATGTCCCCGCGGCTG (CHRNE) NP_000071.1:p.His336=
XM_011523612.1:c.-289_-270delinsCAGCCGCGGGGACATGGCGT (C17orf107) XP_011521914.1:n.-289_-270delinsCAGCCGCGGGGACATGGCGT
NM_000080.4:c.1007_1026delinsACGCCATGTCCCCGCGGCTG (CHRNE) MANE Select NP_000071.1:p.His336=
XM_017024115.1:c.971_990delinsACGCCATGTCCCCGCGGCTG (CHRNE) XP_016879604.1:p.His324=
XR_001752421.1:n.1737_1756delinsACGCCATGTCCCCGCGGCTG (CHRNE)