Canonical Allele Identifier: CA2808296106
Gene: CHRNE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898128dup , CM000679.2:g.4898128dup GRCh38
NC_000017.10:g.4801423dup , CM000679.1:g.4801423dup GRCh37
NC_000017.9:g.4742202dup NCBI36
NG_008029.2:g.9951dup
NG_028005.1:g.69789dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*611dup MANE Select ENSP00000497829.1:n.*611dup
ENST00000649830.1:c.*729dup ENSP00000496907.1:n.*729dup
ENST00000652550.1:n.1819dup
ENST00000293780.4:c.*611dup ENSP00000293780.4:n.*611dup
ENST00000572438.1:n.1779dup
NM_000080.3:c.*611dup NP_000071.1:n.*611dup
NM_000080.4:c.*611dup MANE Select NP_000071.1:n.*611dup
XM_017024115.1:c.*611dup XP_016879604.1:n.*611dup