Canonical Allele Identifier: CA2653783751

Gene: CHRNA4

Linked Data

• gnomAD v4: 20-63350580-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350581del , CM000682.2:g.63350581del	GRCh38
NC_000020.10:g.61981933del , CM000682.1:g.61981933del	GRCh37
NC_000020.9:g.61452377del	NCBI36
NG_011931.1:g.15763del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.830del MANE Select	ENSP00000359285.4:p.Leu277ArgfsTer?
ENST00000370263.8:c.830del	ENSP00000359285.4:p.Leu277ArgfsTer?
ENST00000463705.5:n.1478del
ENST00000467563.3:n.900del
ENST00000498043.6:c.854del
ENST00000615287.4:c.617del	ENSP00000483388.1:p.Leu206ArgfsTer?
ENST00000627000.1:c.*519del	ENSP00000486914.1:n.*519del
ENST00000630240.1:n.551del
NM_000744.6:c.830del	NP_000735.1:p.Leu277ArgfsTer?
NM_001256573.1:c.302del	NP_001243502.1:p.Leu101ArgfsTer?
NR_046317.1:n.1086del
XM_011528524.1:c.617del	XP_011526826.1:p.Leu206ArgfsTer?
XM_017027625.2:c.302del	XP_016883114.1:p.Leu101ArgfsTer?
XM_024451822.1:c.302del	XP_024307590.1:p.Leu101ArgfsTer?
NM_001256573.2:c.302del	NP_001243502.1:p.Leu101ArgfsTer?
NR_046317.2:n.1039del
NM_000744.7:c.830del MANE Select	NP_000735.1:p.Leu277ArgfsTer?