Canonical Allele Identifier: CA2653785244

Gene: CHRNA4

Linked Data

• gnomAD v4: 20-63350926-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350927del , CM000682.2:g.63350927del	GRCh38
NC_000020.10:g.61982279del , CM000682.1:g.61982279del	GRCh37
NC_000020.9:g.61452723del	NCBI36
NG_011931.1:g.15417del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.484del MANE Select	ENSP00000359285.4:p.Ser162AlafsTer16
ENST00000370263.8:c.484del	ENSP00000359285.4:p.Ser162AlafsTer16
ENST00000463705.5:n.1132del
ENST00000467563.3:n.554del
ENST00000498043.6:c.508del
ENST00000615287.4:c.271del	ENSP00000483388.1:p.Ser91AlafsTer16
ENST00000627000.1:c.*173del	ENSP00000486914.1:n.*173del
ENST00000628665.1:n.527del
ENST00000630240.1:n.205del
NM_000744.6:c.484del	NP_000735.1:p.Ser162AlafsTer16
NM_001256573.1:c.-45del	NP_001243502.1:n.-45del
NR_046317.1:n.740del
XM_011528524.1:c.271del	XP_011526826.1:p.Ser91AlafsTer16
XM_017027625.2:c.-45del	XP_016883114.1:n.-45del
XM_024451822.1:c.-45del	XP_024307590.1:n.-45del
NM_001256573.2:c.-45del	NP_001243502.1:n.-45del
NR_046317.2:n.693del
NM_000744.7:c.484del MANE Select	NP_000735.1:p.Ser162AlafsTer16