Canonical Allele Identifier: CA2244610875
Gene: CHRNE HGNC NCBI
C17orf107 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4899425A= , CM000679.2:g.4899425A= GRCh38
NC_000017.10:g.4802720A= , CM000679.1:g.4802720A= GRCh37
NC_000017.9:g.4743499A= NCBI36
NG_008029.2:g.8651T=
NG_028005.1:g.71086A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.1033-41T= (CHRNE) MANE Select ENSP00000497829.1:n.1033-41T=
ENST00000649830.1:c.100-41T= (CHRNE) ENSP00000496907.1:n.100-41T=
ENST00000652550.1:n.763-41T= (CHRNE)
ENST00000293780.4:c.1033-41T= (CHRNE) ENSP00000293780.4:n.1033-41T=
ENST00000521575.1:c.-338A= (C17orf107) ENSP00000429241.1:n.-338A=
ENST00000572438.1:n.719-41T= (CHRNE)
NM_000080.3:c.1033-41T= (CHRNE) NP_000071.1:n.1033-41T=
NM_000080.4:c.1033-41T= (CHRNE) MANE Select NP_000071.1:n.1033-41T=
XM_017024115.1:c.997-41T= (CHRNE) XP_016879604.1:n.997-41T=
XR_001752421.1:n.1763-41T= (CHRNE)