Canonical Allele Identifier: CA16620947

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63346830T>C , CM000682.2:g.63346830T>C	GRCh38
NC_000020.10:g.61978182T>C , CM000682.1:g.61978182T>C	GRCh37
NC_000020.9:g.61448626T>C	NCBI36
NG_011931.1:g.19514A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1792A>G MANE Select	ENSP00000359285.4:p.Ile598Val
ENST00000370263.8:c.1792A>G	ENSP00000359285.4:p.Ile598Val
ENST00000463705.5:n.2440A>G
ENST00000467563.3:n.1862A>G
ENST00000498043.6:c.1816A>G
ENST00000615287.4:c.1579A>G	ENSP00000483388.1:p.Ile527Val
ENST00000627000.1:c.*1481A>G	ENSP00000486914.1:n.*1481A>G
ENST00000631289.1:n.106A>G
NM_000744.6:c.1792A>G	NP_000735.1:p.Ile598Val
NM_001256573.1:c.1264A>G	NP_001243502.1:p.Ile422Val
NR_046317.1:n.2048A>G
XM_011528524.1:c.1579A>G	XP_011526826.1:p.Ile527Val
XM_017027625.2:c.1264A>G	XP_016883114.1:p.Ile422Val
XM_024451822.1:c.1264A>G	XP_024307590.1:p.Ile422Val
NM_001256573.2:c.1264A>G	NP_001243502.1:p.Ile422Val
NR_046317.2:n.2001A>G
NM_000744.7:c.1792A>G MANE Select	NP_000735.1:p.Ile598Val