Canonical Allele Identifier: CA2653783300

Gene: CHRNA4

Linked Data

• gnomAD v4: 20-63350415-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350416del , CM000682.2:g.63350416del	GRCh38
NC_000020.10:g.61981768del , CM000682.1:g.61981768del	GRCh37
NC_000020.9:g.61452212del	NCBI36
NG_011931.1:g.15928del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.995del MANE Select	ENSP00000359285.4:p.His332ProfsTer27
ENST00000370263.8:c.995del	ENSP00000359285.4:p.His332ProfsTer27
ENST00000463705.5:n.1643del
ENST00000467563.3:n.1065del
ENST00000498043.6:c.1019del
ENST00000615287.4:c.782del	ENSP00000483388.1:p.His261ProfsTer27
ENST00000627000.1:c.*684del	ENSP00000486914.1:n.*684del
ENST00000630240.1:n.716del
NM_000744.6:c.995del	NP_000735.1:p.His332ProfsTer27
NM_001256573.1:c.467del	NP_001243502.1:p.His156ProfsTer27
NR_046317.1:n.1251del
XM_011528524.1:c.782del	XP_011526826.1:p.His261ProfsTer27
XM_017027625.2:c.467del	XP_016883114.1:p.His156ProfsTer27
XM_024451822.1:c.467del	XP_024307590.1:p.His156ProfsTer27
NM_001256573.2:c.467del	NP_001243502.1:p.His156ProfsTer27
NR_046317.2:n.1204del
NM_000744.7:c.995del MANE Select	NP_000735.1:p.His332ProfsTer27