Canonical Allele Identifier: CA2244610171
Gene: CHRNE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898555A= , CM000679.2:g.4898555A= GRCh38
NC_000017.10:g.4801850A= , CM000679.1:g.4801850A= GRCh37
NC_000017.9:g.4742629A= NCBI36
NG_008029.2:g.9521T=
NG_028005.1:g.70216A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*181T= MANE Select ENSP00000497829.1:n.*181T=
ENST00000649830.1:c.*299T= ENSP00000496907.1:n.*299T=
ENST00000652550.1:n.1389T=
ENST00000293780.4:c.*181T= ENSP00000293780.4:n.*181T=
ENST00000572438.1:n.1349T=
NM_000080.3:c.*181T= NP_000071.1:n.*181T=
NM_000080.4:c.*181T= MANE Select NP_000071.1:n.*181T=
XM_017024115.1:c.*181T= XP_016879604.1:n.*181T=