Canonical Allele Identifier: CA2244610287
Gene: CHRNE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898710G= , CM000679.2:g.4898710G= GRCh38
NC_000017.10:g.4802005G= , CM000679.1:g.4802005G= GRCh37
NC_000017.9:g.4742784G= NCBI36
NG_008029.2:g.9366C=
NG_028005.1:g.70371G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*26C= MANE Select ENSP00000497829.1:n.*26C=
ENST00000649830.1:c.*144C= ENSP00000496907.1:n.*144C=
ENST00000652550.1:n.1234C=
ENST00000293780.4:c.*26C= ENSP00000293780.4:n.*26C=
ENST00000572438.1:n.1194C=
NM_000080.3:c.*26C= NP_000071.1:n.*26C=
NM_000080.4:c.*26C= MANE Select NP_000071.1:n.*26C=
XM_017024115.1:c.*26C= XP_016879604.1:n.*26C=