Canonical Allele Identifier: CA2244610290
Gene: CHRNE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898712G= , CM000679.2:g.4898712G= GRCh38
NC_000017.10:g.4802007G= , CM000679.1:g.4802007G= GRCh37
NC_000017.9:g.4742786G= NCBI36
NG_008029.2:g.9364C=
NG_028005.1:g.70373G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*24C= MANE Select ENSP00000497829.1:n.*24C=
ENST00000649830.1:c.*142C= ENSP00000496907.1:n.*142C=
ENST00000652550.1:n.1232C=
ENST00000293780.4:c.*24C= ENSP00000293780.4:n.*24C=
ENST00000572438.1:n.1192C=
NM_000080.3:c.*24C= NP_000071.1:n.*24C=
NM_000080.4:c.*24C= MANE Select NP_000071.1:n.*24C=
XM_017024115.1:c.*24C= XP_016879604.1:n.*24C=
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