Canonical Allele Identifier: CA2244610082
Gene: CHRNE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898404T= , CM000679.2:g.4898404T= GRCh38
NC_000017.10:g.4801699T= , CM000679.1:g.4801699T= GRCh37
NC_000017.9:g.4742478T= NCBI36
NG_008029.2:g.9672A=
NG_028005.1:g.70065T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*332A= MANE Select ENSP00000497829.1:n.*332A=
ENST00000649830.1:c.*450A= ENSP00000496907.1:n.*450A=
ENST00000652550.1:n.1540A=
ENST00000293780.4:c.*332A= ENSP00000293780.4:n.*332A=
ENST00000572438.1:n.1500A=
NM_000080.3:c.*332A= NP_000071.1:n.*332A=
NM_000080.4:c.*332A= MANE Select NP_000071.1:n.*332A=
XM_017024115.1:c.*332A= XP_016879604.1:n.*332A=
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