Canonical Allele Identifier: CA1019264326

Gene: CHRNA4

Linked Data

• gnomAD v3: 20-63350738-AC-A
• gnomAD v4: 20-63350738-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350739del , CM000682.2:g.63350739del	GRCh38
NC_000020.10:g.61982091del , CM000682.1:g.61982091del	GRCh37
NC_000020.9:g.61452535del	NCBI36
NG_011931.1:g.15605del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370263.9:c.672del MANE Select	ENSP00000359285.4:p.Glu224AspfsTer?
ENST00000370263.8:c.672del	ENSP00000359285.4:p.Glu224AspfsTer?
ENST00000463705.5:n.1320del
ENST00000467563.3:n.742del
ENST00000498043.6:c.696del
ENST00000615287.4:c.459del	ENSP00000483388.1:p.Glu153AspfsTer?
ENST00000627000.1:c.*361del	ENSP00000486914.1:n.*361del
ENST00000630240.1:n.393del
NM_000744.6:c.672del	NP_000735.1:p.Glu224AspfsTer?
NM_001256573.1:c.144del	NP_001243502.1:p.Glu48AspfsTer?
NR_046317.1:n.928del
XM_011528524.1:c.459del	XP_011526826.1:p.Glu153AspfsTer?
XM_017027625.2:c.144del	XP_016883114.1:p.Glu48AspfsTer?
XM_024451822.1:c.144del	XP_024307590.1:p.Glu48AspfsTer?
NM_001256573.2:c.144del	NP_001243502.1:p.Glu48AspfsTer?
NR_046317.2:n.881del
NM_000744.7:c.672del MANE Select	NP_000735.1:p.Glu224AspfsTer?