Canonical Allele Identifier: CA2244609880
Gene: CHRNE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898123G= , CM000679.2:g.4898123G= GRCh38
NC_000017.10:g.4801418G= , CM000679.1:g.4801418G= GRCh37
NC_000017.9:g.4742197G= NCBI36
NG_008029.2:g.9953C=
NG_028005.1:g.69784G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*613C= MANE Select ENSP00000497829.1:n.*613C=
ENST00000649830.1:c.*731C= ENSP00000496907.1:n.*731C=
ENST00000652550.1:n.1821C=
ENST00000293780.4:c.*613C= ENSP00000293780.4:n.*613C=
ENST00000572438.1:n.1781C=
NM_000080.3:c.*613C= NP_000071.1:n.*613C=
NM_000080.4:c.*613C= MANE Select NP_000071.1:n.*613C=
XM_017024115.1:c.*613C= XP_016879604.1:n.*613C=
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