Canonical Allele Identifier: CA1019264223
Gene: CHRNA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350731_63350732insTGGTCG , CM000682.2:g.63350731_63350732insTGGTCG GRCh38
NC_000020.10:g.61982083_61982084insTGGTCG , CM000682.1:g.61982083_61982084insTGGTCG GRCh37
NC_000020.9:g.61452527_61452528insTGGTCG NCBI36
NG_011931.1:g.15613_15614insGACCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000370263.9:c.680_681insGACCAC MANE Select ENSP00000359285.4:p.Ala227_Glu228insThrThr
ENST00000370263.8:c.680_681insGACCAC ENSP00000359285.4:p.Ala227_Glu228insThrThr
ENST00000463705.5:n.1328_1329insGACCAC
ENST00000467563.3:n.750_751insGACCAC
ENST00000498043.6:c.704_705insGACCAC
ENST00000615287.4:c.467_468insGACCAC ENSP00000483388.1:p.Ala156_Glu157insThrThr
ENST00000627000.1:c.*369_*370insGACCAC ENSP00000486914.1:n.*369_*370insGACCAC
ENST00000630240.1:n.401_402insGACCAC
NM_000744.6:c.680_681insGACCAC NP_000735.1:p.Ala227_Glu228insThrThr
NM_001256573.1:c.152_153insGACCAC NP_001243502.1:p.Ala51_Glu52insThrThr
NR_046317.1:n.936_937insGACCAC
XM_011528524.1:c.467_468insGACCAC XP_011526826.1:p.Ala156_Glu157insThrThr
XM_017027625.2:c.152_153insGACCAC XP_016883114.1:p.Ala51_Glu52insThrThr
XM_024451822.1:c.152_153insGACCAC XP_024307590.1:p.Ala51_Glu52insThrThr
NM_001256573.2:c.152_153insGACCAC NP_001243502.1:p.Ala51_Glu52insThrThr
NR_046317.2:n.889_890insGACCAC
NM_000744.7:c.680_681insGACCAC MANE Select NP_000735.1:p.Ala227_Glu228insThrThr