Canonical Allele Identifier: CA409637616
Gene: CHRNA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350803A>T , CM000682.2:g.63350803A>T GRCh38
NC_000020.10:g.61982155A>T , CM000682.1:g.61982155A>T GRCh37
NC_000020.9:g.61452599A>T NCBI36
NG_011931.1:g.15541T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370263.9:c.608T>A MANE Select ENSP00000359285.4:p.Phe203Tyr
ENST00000370263.8:c.608T>A ENSP00000359285.4:p.Phe203Tyr
ENST00000463705.5:n.1256T>A
ENST00000467563.3:n.678T>A
ENST00000498043.6:c.632T>A
ENST00000615287.4:c.395T>A ENSP00000483388.1:p.Phe132Tyr
ENST00000627000.1:c.*297T>A ENSP00000486914.1:n.*297T>A
ENST00000630240.1:n.329T>A
NM_000744.6:c.608T>A NP_000735.1:p.Phe203Tyr
NM_001256573.1:c.80T>A NP_001243502.1:p.Phe27Tyr
NR_046317.1:n.864T>A
XM_011528524.1:c.395T>A XP_011526826.1:p.Phe132Tyr
XM_017027625.2:c.80T>A XP_016883114.1:p.Phe27Tyr
XM_024451822.1:c.80T>A XP_024307590.1:p.Phe27Tyr
NM_001256573.2:c.80T>A NP_001243502.1:p.Phe27Tyr
NR_046317.2:n.817T>A
NM_000744.7:c.608T>A MANE Select NP_000735.1:p.Phe203Tyr