Canonical Allele Identifier: CA636613626
Gene: CHRNA4 HGNC NCBI

Linked Data

dbSNP Id: rs1568809240

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350308_63350310del , CM000682.2:g.63350308_63350310del GRCh38
NC_000020.10:g.61981660_61981662del , CM000682.1:g.61981660_61981662del GRCh37
NC_000020.9:g.61452104_61452106del NCBI36
NG_011931.1:g.16034_16036del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370263.9:c.1101_1103del MANE Select ENSP00000359285.4:p.Cys368del
ENST00000370263.8:c.1101_1103del ENSP00000359285.4:p.Cys368del
ENST00000463705.5:n.1749_1751del
ENST00000467563.3:n.1171_1173del
ENST00000498043.6:c.1125_1127del
ENST00000615287.4:c.888_890del ENSP00000483388.1:p.Cys297del
ENST00000627000.1:c.*790_*792del ENSP00000486914.1:n.*790_*792del
ENST00000630240.1:n.822_824del
NM_000744.6:c.1101_1103del NP_000735.1:p.Cys368del
NM_001256573.1:c.573_575del NP_001243502.1:p.Cys192del
NR_046317.1:n.1357_1359del
XM_011528524.1:c.888_890del XP_011526826.1:p.Cys297del
XM_017027625.2:c.573_575del XP_016883114.1:p.Cys192del
XM_024451822.1:c.573_575del XP_024307590.1:p.Cys192del
NM_001256573.2:c.573_575del NP_001243502.1:p.Cys192del
NR_046317.2:n.1310_1312del
NM_000744.7:c.1101_1103del MANE Select NP_000735.1:p.Cys368del