Canonical Allele Identifier: CA2244610143
Gene: CHRNE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898502G= , CM000679.2:g.4898502G= GRCh38
NC_000017.10:g.4801797G= , CM000679.1:g.4801797G= GRCh37
NC_000017.9:g.4742576G= NCBI36
NG_008029.2:g.9574C=
NG_028005.1:g.70163G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*234C= MANE Select ENSP00000497829.1:n.*234C=
ENST00000649830.1:c.*352C= ENSP00000496907.1:n.*352C=
ENST00000652550.1:n.1442C=
ENST00000293780.4:c.*234C= ENSP00000293780.4:n.*234C=
ENST00000572438.1:n.1402C=
NM_000080.3:c.*234C= NP_000071.1:n.*234C=
NM_000080.4:c.*234C= MANE Select NP_000071.1:n.*234C=
XM_017024115.1:c.*234C= XP_016879604.1:n.*234C=
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