Canonical Allele Identifier: CA2244610308
Gene: CHRNE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898734A= , CM000679.2:g.4898734A= GRCh38
NC_000017.10:g.4802029A= , CM000679.1:g.4802029A= GRCh37
NC_000017.9:g.4742808A= NCBI36
NG_008029.2:g.9342T=
NG_028005.1:g.70395A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*2T= MANE Select ENSP00000497829.1:n.*2T=
ENST00000649830.1:c.*120T= ENSP00000496907.1:n.*120T=
ENST00000652550.1:n.1210T=
ENST00000293780.4:c.*2T= ENSP00000293780.4:n.*2T=
ENST00000572438.1:n.1170T=
NM_000080.3:c.*2T= NP_000071.1:n.*2T=
NM_000080.4:c.*2T= MANE Select NP_000071.1:n.*2T=
XM_017024115.1:c.*2T= XP_016879604.1:n.*2T=