Canonical Allele Identifier: CA2244610276
Gene: CHRNE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898700T= , CM000679.2:g.4898700T= GRCh38
NC_000017.10:g.4801995T= , CM000679.1:g.4801995T= GRCh37
NC_000017.9:g.4742774T= NCBI36
NG_008029.2:g.9376A=
NG_028005.1:g.70361T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*36A= MANE Select ENSP00000497829.1:n.*36A=
ENST00000649830.1:c.*154A= ENSP00000496907.1:n.*154A=
ENST00000652550.1:n.1244A=
ENST00000293780.4:c.*36A= ENSP00000293780.4:n.*36A=
ENST00000572438.1:n.1204A=
NM_000080.3:c.*36A= NP_000071.1:n.*36A=
NM_000080.4:c.*36A= MANE Select NP_000071.1:n.*36A=
XM_017024115.1:c.*36A= XP_016879604.1:n.*36A=