Canonical Allele Identifier: CA2816988850

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350731_63350732insTGGAGGC , CM000682.2:g.63350731_63350732insTGGAGGC	GRCh38
NC_000020.10:g.61982083_61982084insTGGAGGC , CM000682.1:g.61982083_61982084insTGGAGGC	GRCh37
NC_000020.9:g.61452527_61452528insTGGAGGC	NCBI36
NG_011931.1:g.15612_15613insGCCTCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.679_680insGCCTCCA MANE Select	ENSP00000359285.4:p.Ala227GlyfsTer?
ENST00000370263.8:c.679_680insGCCTCCA	ENSP00000359285.4:p.Ala227GlyfsTer?
ENST00000463705.5:n.1327_1328insGCCTCCA
ENST00000467563.3:n.749_750insGCCTCCA
ENST00000498043.6:c.703_704insGCCTCCA
ENST00000615287.4:c.466_467insGCCTCCA	ENSP00000483388.1:p.Ala156GlyfsTer?
ENST00000627000.1:c.*368_*369insGCCTCCA	ENSP00000486914.1:n.*368_*369insGCCTCCA
ENST00000630240.1:n.400_401insGCCTCCA
NM_000744.6:c.679_680insGCCTCCA	NP_000735.1:p.Ala227GlyfsTer?
NM_001256573.1:c.151_152insGCCTCCA	NP_001243502.1:p.Ala51GlyfsTer?
NR_046317.1:n.935_936insGCCTCCA
XM_011528524.1:c.466_467insGCCTCCA	XP_011526826.1:p.Ala156GlyfsTer?
XM_017027625.2:c.151_152insGCCTCCA	XP_016883114.1:p.Ala51GlyfsTer?
XM_024451822.1:c.151_152insGCCTCCA	XP_024307590.1:p.Ala51GlyfsTer?
NM_001256573.2:c.151_152insGCCTCCA	NP_001243502.1:p.Ala51GlyfsTer?
NR_046317.2:n.888_889insGCCTCCA
NM_000744.7:c.679_680insGCCTCCA MANE Select	NP_000735.1:p.Ala227GlyfsTer?