Canonical Allele Identifier: CA2635579122
Gene: CHRNE HGNC NCBI
C17orf107 HGNC NCBI

Linked Data

gnomAD v4: 17-4899426-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4899426G>T , CM000679.2:g.4899426G>T GRCh38
NC_000017.10:g.4802721G>T , CM000679.1:g.4802721G>T GRCh37
NC_000017.9:g.4743500G>T NCBI36
NG_008029.2:g.8650C>A
NG_028005.1:g.71087G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.1033-42C>A (CHRNE) MANE Select ENSP00000497829.1:n.1033-42C>A
ENST00000649830.1:c.100-42C>A (CHRNE) ENSP00000496907.1:n.100-42C>A
ENST00000652550.1:n.763-42C>A (CHRNE)
ENST00000293780.4:c.1033-42C>A (CHRNE) ENSP00000293780.4:n.1033-42C>A
ENST00000521575.1:c.-337G>T (C17orf107) ENSP00000429241.1:n.-337G>T
ENST00000572438.1:n.719-42C>A (CHRNE)
NM_000080.3:c.1033-42C>A (CHRNE) NP_000071.1:n.1033-42C>A
NM_000080.4:c.1033-42C>A (CHRNE) MANE Select NP_000071.1:n.1033-42C>A
XM_017024115.1:c.997-42C>A (CHRNE) XP_016879604.1:n.997-42C>A
XR_001752421.1:n.1763-42C>A (CHRNE)