Canonical Allele Identifier: CA409637861
Gene: CHRNA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350842T>A , CM000682.2:g.63350842T>A GRCh38
NC_000020.10:g.61982194T>A , CM000682.1:g.61982194T>A GRCh37
NC_000020.9:g.61452638T>A NCBI36
NG_011931.1:g.15502A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370263.9:c.569A>T MANE Select ENSP00000359285.4:p.Asp190Val
ENST00000370263.8:c.569A>T ENSP00000359285.4:p.Asp190Val
ENST00000463705.5:n.1217A>T
ENST00000467563.3:n.639A>T
ENST00000498043.6:c.593A>T
ENST00000615287.4:c.356A>T ENSP00000483388.1:p.Asp119Val
ENST00000627000.1:c.*258A>T ENSP00000486914.1:n.*258A>T
ENST00000630240.1:n.290A>T
NM_000744.6:c.569A>T NP_000735.1:p.Asp190Val
NM_001256573.1:c.41A>T NP_001243502.1:p.Asp14Val
NR_046317.1:n.825A>T
XM_011528524.1:c.356A>T XP_011526826.1:p.Asp119Val
XM_017027625.2:c.41A>T XP_016883114.1:p.Asp14Val
XM_024451822.1:c.41A>T XP_024307590.1:p.Asp14Val
NM_001256573.2:c.41A>T NP_001243502.1:p.Asp14Val
NR_046317.2:n.778A>T
NM_000744.7:c.569A>T MANE Select NP_000735.1:p.Asp190Val