Canonical Allele Identifier: CA2244610204
Gene: CHRNE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898615A= , CM000679.2:g.4898615A= GRCh38
NC_000017.10:g.4801910A= , CM000679.1:g.4801910A= GRCh37
NC_000017.9:g.4742689A= NCBI36
NG_008029.2:g.9461T=
NG_028005.1:g.70276A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*121T= MANE Select ENSP00000497829.1:n.*121T=
ENST00000649830.1:c.*239T= ENSP00000496907.1:n.*239T=
ENST00000652550.1:n.1329T=
ENST00000293780.4:c.*121T= ENSP00000293780.4:n.*121T=
ENST00000572438.1:n.1289T=
NM_000080.3:c.*121T= NP_000071.1:n.*121T=
NM_000080.4:c.*121T= MANE Select NP_000071.1:n.*121T=
XM_017024115.1:c.*121T= XP_016879604.1:n.*121T=