Canonical Allele Identifier: CA2244610320
Gene: CHRNE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898753G= , CM000679.2:g.4898753G= GRCh38
NC_000017.10:g.4802048G= , CM000679.1:g.4802048G= GRCh37
NC_000017.9:g.4742827G= NCBI36
NG_008029.2:g.9323C=
NG_028005.1:g.70414G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.1465C= MANE Select ENSP00000497829.1:p.Pro489=
ENST00000649830.1:c.*101C= ENSP00000496907.1:n.*101C=
ENST00000652550.1:n.1191C=
ENST00000293780.4:c.1465C= ENSP00000293780.4:p.Pro489=
ENST00000572438.1:n.1151C=
NM_000080.3:c.1465C= NP_000071.1:p.Pro489=
NM_000080.4:c.1465C= MANE Select NP_000071.1:p.Pro489=
XM_017024115.1:c.1429C= XP_016879604.1:p.Pro477=