Canonical Allele Identifier: CA2581289341
Gene: CHRNE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898699C>G , CM000679.2:g.4898699C>G GRCh38
NC_000017.10:g.4801994C>G , CM000679.1:g.4801994C>G GRCh37
NC_000017.9:g.4742773C>G NCBI36
NG_008029.2:g.9377G>C
NG_028005.1:g.70360C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*37G>C MANE Select ENSP00000497829.1:n.*37G>C
ENST00000649830.1:c.*155G>C ENSP00000496907.1:n.*155G>C
ENST00000652550.1:n.1245G>C
ENST00000293780.4:c.*37G>C ENSP00000293780.4:n.*37G>C
ENST00000572438.1:n.1205G>C
NM_000080.3:c.*37G>C NP_000071.1:n.*37G>C
NM_000080.4:c.*37G>C MANE Select NP_000071.1:n.*37G>C
XM_017024115.1:c.*37G>C XP_016879604.1:n.*37G>C
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