Canonical Allele Identifier: CA2244610300
Gene: CHRNE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898728G= , CM000679.2:g.4898728G= GRCh38
NC_000017.10:g.4802023G= , CM000679.1:g.4802023G= GRCh37
NC_000017.9:g.4742802G= NCBI36
NG_008029.2:g.9348C=
NG_028005.1:g.70389G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*8C= MANE Select ENSP00000497829.1:n.*8C=
ENST00000649830.1:c.*126C= ENSP00000496907.1:n.*126C=
ENST00000652550.1:n.1216C=
ENST00000293780.4:c.*8C= ENSP00000293780.4:n.*8C=
ENST00000572438.1:n.1176C=
NM_000080.3:c.*8C= NP_000071.1:n.*8C=
NM_000080.4:c.*8C= MANE Select NP_000071.1:n.*8C=
XM_017024115.1:c.*8C= XP_016879604.1:n.*8C=