Canonical Allele Identifier: CA2244610350
Gene: CHRNE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898801T= , CM000679.2:g.4898801T= GRCh38
NC_000017.10:g.4802096T= , CM000679.1:g.4802096T= GRCh37
NC_000017.9:g.4742875T= NCBI36
NG_008029.2:g.9275A=
NG_028005.1:g.70462T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.1417A= MANE Select ENSP00000497829.1:p.Ile473=
ENST00000649830.1:c.*53A= ENSP00000496907.1:n.*53A=
ENST00000652550.1:n.1143A=
ENST00000293780.4:c.1417A= ENSP00000293780.4:p.Ile473=
ENST00000572438.1:n.1103A=
NM_000080.3:c.1417A= NP_000071.1:p.Ile473=
NM_000080.4:c.1417A= MANE Select NP_000071.1:p.Ile473=
XM_017024115.1:c.1381A= XP_016879604.1:p.Ile461=