Canonical Allele Identifier: CA2244609873
Gene: CHRNE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898116C= , CM000679.2:g.4898116C= GRCh38
NC_000017.10:g.4801411C= , CM000679.1:g.4801411C= GRCh37
NC_000017.9:g.4742190C= NCBI36
NG_008029.2:g.9960G=
NG_028005.1:g.69777C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*620G= MANE Select ENSP00000497829.1:n.*620G=
ENST00000649830.1:c.*738G= ENSP00000496907.1:n.*738G=
ENST00000652550.1:n.1828G=
ENST00000293780.4:c.*620G= ENSP00000293780.4:n.*620G=
ENST00000572438.1:n.1788G=
NM_000080.3:c.*620G= NP_000071.1:n.*620G=
NM_000080.4:c.*620G= MANE Select NP_000071.1:n.*620G=
XM_017024115.1:c.*620G= XP_016879604.1:n.*620G=