Canonical Allele Identifier: CA2244610309
Gene: CHRNE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898738A= , CM000679.2:g.4898738A= GRCh38
NC_000017.10:g.4802033A= , CM000679.1:g.4802033A= GRCh37
NC_000017.9:g.4742812A= NCBI36
NG_008029.2:g.9338T=
NG_028005.1:g.70399A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.1480T= MANE Select ENSP00000497829.1:p.Ter494=
ENST00000649830.1:c.*116T= ENSP00000496907.1:n.*116T=
ENST00000652550.1:n.1206T=
ENST00000293780.4:c.1480T= ENSP00000293780.4:p.Ter494=
ENST00000572438.1:n.1166T=
NM_000080.3:c.1480T= NP_000071.1:p.Ter494=
NM_000080.4:c.1480T= MANE Select NP_000071.1:p.Ter494=
XM_017024115.1:c.1444T= XP_016879604.1:p.Ter482=