Canonical Allele Identifier: CA2244609899
Gene: CHRNE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898145G= , CM000679.2:g.4898145G= GRCh38
NC_000017.10:g.4801440G= , CM000679.1:g.4801440G= GRCh37
NC_000017.9:g.4742219G= NCBI36
NG_008029.2:g.9931C=
NG_028005.1:g.69806G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*591C= MANE Select ENSP00000497829.1:n.*591C=
ENST00000649830.1:c.*709C= ENSP00000496907.1:n.*709C=
ENST00000652550.1:n.1799C=
ENST00000293780.4:c.*591C= ENSP00000293780.4:n.*591C=
ENST00000572438.1:n.1759C=
NM_000080.3:c.*591C= NP_000071.1:n.*591C=
NM_000080.4:c.*591C= MANE Select NP_000071.1:n.*591C=
XM_017024115.1:c.*591C= XP_016879604.1:n.*591C=
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