Canonical Allele Identifier: CA2576135495
Gene: CHRNE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898644G>C , CM000679.2:g.4898644G>C GRCh38
NC_000017.10:g.4801939G>C , CM000679.1:g.4801939G>C GRCh37
NC_000017.9:g.4742718G>C NCBI36
NG_008029.2:g.9432C>G
NG_028005.1:g.70305G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*92C>G MANE Select ENSP00000497829.1:n.*92C>G
ENST00000649830.1:c.*210C>G ENSP00000496907.1:n.*210C>G
ENST00000652550.1:n.1300C>G
ENST00000293780.4:c.*92C>G ENSP00000293780.4:n.*92C>G
ENST00000572438.1:n.1260C>G
NM_000080.3:c.*92C>G NP_000071.1:n.*92C>G
NM_000080.4:c.*92C>G MANE Select NP_000071.1:n.*92C>G
XM_017024115.1:c.*92C>G XP_016879604.1:n.*92C>G