Canonical Allele Identifier: CA2374743133

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350732_63350735delinsCACA , CM000682.2:g.63350732_63350735delinsCACA	GRCh38
NC_000020.10:g.61982084_61982087delinsCACA , CM000682.1:g.61982084_61982087delinsCACA	GRCh37
NC_000020.9:g.61452528_61452531delinsCACA	NCBI36
NG_011931.1:g.15609_15612delinsTGTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000370263.9:c.676_679delinsTGTG MANE Select	ENSP00000359285.4:p.Cys226=
ENST00000370263.8:c.676_679delinsTGTG	ENSP00000359285.4:p.Cys226=
ENST00000463705.5:n.1324_1327delinsTGTG
ENST00000467563.3:n.746_749delinsTGTG
ENST00000498043.6:c.700_703delinsTGTG
ENST00000615287.4:c.463_466delinsTGTG	ENSP00000483388.1:p.Cys155=
ENST00000627000.1:c.*365_*368delinsTGTG	ENSP00000486914.1:n.*365_*368delinsTGTG
ENST00000630240.1:n.397_400delinsTGTG
NM_000744.6:c.676_679delinsTGTG	NP_000735.1:p.Cys226=
NM_001256573.1:c.148_151delinsTGTG	NP_001243502.1:p.Cys50=
NR_046317.1:n.932_935delinsTGTG
XM_011528524.1:c.463_466delinsTGTG	XP_011526826.1:p.Cys155=
XM_017027625.2:c.148_151delinsTGTG	XP_016883114.1:p.Cys50=
XM_024451822.1:c.148_151delinsTGTG	XP_024307590.1:p.Cys50=
NM_001256573.2:c.148_151delinsTGTG	NP_001243502.1:p.Cys50=
NR_046317.2:n.885_888delinsTGTG
NM_000744.7:c.676_679delinsTGTG MANE Select	NP_000735.1:p.Cys226=