Canonical Allele Identifier: CA2842938891

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350731_63350732insTGGTGG , CM000682.2:g.63350731_63350732insTGGTGG	GRCh38
NC_000020.10:g.61982083_61982084insTGGTGG , CM000682.1:g.61982083_61982084insTGGTGG	GRCh37
NC_000020.9:g.61452527_61452528insTGGTGG	NCBI36
NG_011931.1:g.15614_15615insACCACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.681_682insACCACC MANE Select	ENSP00000359285.4:p.Ala227_Glu228insThrThr
ENST00000370263.8:c.681_682insACCACC	ENSP00000359285.4:p.Ala227_Glu228insThrThr
ENST00000463705.5:n.1329_1330insACCACC
ENST00000467563.3:n.751_752insACCACC
ENST00000498043.6:c.705_706insACCACC
ENST00000615287.4:c.468_469insACCACC	ENSP00000483388.1:p.Ala156_Glu157insThrThr
ENST00000627000.1:c.*370_*371insACCACC	ENSP00000486914.1:n.*370_*371insACCACC
ENST00000630240.1:n.402_403insACCACC
NM_000744.6:c.681_682insACCACC	NP_000735.1:p.Ala227_Glu228insThrThr
NM_001256573.1:c.153_154insACCACC	NP_001243502.1:p.Ala51_Glu52insThrThr
NR_046317.1:n.937_938insACCACC
XM_011528524.1:c.468_469insACCACC	XP_011526826.1:p.Ala156_Glu157insThrThr
XM_017027625.2:c.153_154insACCACC	XP_016883114.1:p.Ala51_Glu52insThrThr
XM_024451822.1:c.153_154insACCACC	XP_024307590.1:p.Ala51_Glu52insThrThr
NM_001256573.2:c.153_154insACCACC	NP_001243502.1:p.Ala51_Glu52insThrThr
NR_046317.2:n.890_891insACCACC
NM_000744.7:c.681_682insACCACC MANE Select	NP_000735.1:p.Ala227_Glu228insThrThr