Canonical Allele Identifier: CA2653789448

Gene: CHRNA4

Linked Data

• gnomAD v4: 20-63349842-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349847del , CM000682.2:g.63349847del	GRCh38
NC_000020.10:g.61981199del , CM000682.1:g.61981199del	GRCh37
NC_000020.9:g.61451643del	NCBI36
NG_011931.1:g.16501del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1568del MANE Select	ENSP00000359285.4:p.Pro523GlnfsTer?
ENST00000370263.8:c.1568del	ENSP00000359285.4:p.Pro523GlnfsTer?
ENST00000463705.5:n.2216del
ENST00000467563.3:n.1638del
ENST00000498043.6:c.1592del
ENST00000615287.4:c.1355del	ENSP00000483388.1:p.Pro452GlnfsTer?
ENST00000627000.1:c.*1257del	ENSP00000486914.1:n.*1257del
ENST00000630240.1:n.1289del
NM_000744.6:c.1568del	NP_000735.1:p.Pro523GlnfsTer?
NM_001256573.1:c.1040del	NP_001243502.1:p.Pro347GlnfsTer?
NR_046317.1:n.1824del
XM_011528524.1:c.1355del	XP_011526826.1:p.Pro452GlnfsTer?
XM_017027625.2:c.1040del	XP_016883114.1:p.Pro347GlnfsTer?
XM_024451822.1:c.1040del	XP_024307590.1:p.Pro347GlnfsTer?
NM_001256573.2:c.1040del	NP_001243502.1:p.Pro347GlnfsTer?
NR_046317.2:n.1777del
NM_000744.7:c.1568del MANE Select	NP_000735.1:p.Pro523GlnfsTer?