Canonical Allele Identifier: CA397306242
Gene: C17orf107 HGNC NCBI
CHRNE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4902017G>T , CM000679.2:g.4902017G>T GRCh38
NC_000017.10:g.4805312G>T , CM000679.1:g.4805312G>T GRCh37
NC_000017.9:g.4746091G>T NCBI36
NG_008029.2:g.6059C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381365.4:c.*1484G>T (C17orf107) MANE Select ENSP00000370770.3:n.*1484G>T
ENST00000649488.2:c.415C>A (CHRNE) MANE Select ENSP00000497829.1:p.Leu139Met
ENST00000649830.1:c.-519C>A (CHRNE) ENSP00000496907.1:n.-519C>A
ENST00000293780.4:c.415C>A (CHRNE) ENSP00000293780.4:p.Leu139Met
ENST00000381365.3:c.*1484G>T (C17orf107) ENSP00000370770.3:n.*1484G>T
ENST00000575637.1:n.236C>A (CHRNE)
NM_000080.3:c.415C>A (CHRNE) NP_000071.1:p.Leu139Met
NM_001145536.1:c.*1484G>T (C17orf107) NP_001139008.1:n.*1484G>T
XM_011523612.1:c.546+1511G>T (C17orf107) XP_011521914.1:n.546+1511G>T
XM_011523631.1:c.415C>A (CHRNE) XP_011521933.1:p.Leu139Met
NM_000080.4:c.415C>A (CHRNE) MANE Select NP_000071.1:p.Leu139Met
XM_017024115.1:c.379C>A (CHRNE) XP_016879604.1:p.Leu127Met
XR_001752421.1:n.1260C>A (CHRNE)
NM_001145536.2:c.*1484G>T (C17orf107) MANE Select NP_001139008.1:n.*1484G>T