Canonical Allele Identifier: CA2244610344
Gene: CHRNE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898790C= , CM000679.2:g.4898790C= GRCh38
NC_000017.10:g.4802085C= , CM000679.1:g.4802085C= GRCh37
NC_000017.9:g.4742864C= NCBI36
NG_008029.2:g.9286G=
NG_028005.1:g.70451C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.1428G= MANE Select ENSP00000497829.1:p.Gly476=
ENST00000649830.1:c.*64G= ENSP00000496907.1:n.*64G=
ENST00000652550.1:n.1154G=
ENST00000293780.4:c.1428G= ENSP00000293780.4:p.Gly476=
ENST00000572438.1:n.1114G=
NM_000080.3:c.1428G= NP_000071.1:p.Gly476=
NM_000080.4:c.1428G= MANE Select NP_000071.1:p.Gly476=
XM_017024115.1:c.1392G= XP_016879604.1:p.Gly464=