Canonical Allele Identifier: CA9957474

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63346719G>A , CM000682.2:g.63346719G>A	GRCh38
NC_000020.10:g.61978071G>A , CM000682.1:g.61978071G>A	GRCh37
NC_000020.9:g.61448515G>A	NCBI36
NG_011931.1:g.19625C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000744.7:c.*19C>T MANE Select	NP_000735.1:n.*19C>T
ENST00000370263.9:c.*19C>T MANE Select	ENSP00000359285.4:n.*19C>T
NM_000744.6:c.*19C>T	NP_000735.1:n.*19C>T
NM_001256573.1:c.*19C>T	NP_001243502.1:n.*19C>T
NM_001256573.2:c.*19C>T	NP_001243502.1:n.*19C>T
NR_046317.1:n.2159C>T
NR_046317.2:n.2112C>T
ENST00000370263.8:c.*19C>T	ENSP00000359285.4:n.*19C>T
ENST00000463705.5:n.2551C>T
ENST00000467563.3:n.1973C>T
ENST00000498043.6:c.1927C>T
ENST00000615287.4:c.*19C>T	ENSP00000483388.1:n.*19C>T
ENST00000627000.1:c.*1592C>T	ENSP00000486914.1:n.*1592C>T
ENST00000631289.1:n.217C>T
XM_011528524.1:c.*19C>T	XP_011526826.1:n.*19C>T
XM_017027625.2:c.*19C>T	XP_016883114.1:n.*19C>T
XM_024451822.1:c.*19C>T	XP_024307590.1:n.*19C>T