Canonical Allele Identifier: CA9957482

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63346781G>A , CM000682.2:g.63346781G>A	GRCh38
NC_000020.10:g.61978133G>A , CM000682.1:g.61978133G>A	GRCh37
NC_000020.9:g.61448577G>A	NCBI36
NG_011931.1:g.19563C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000744.7:c.1841C>T MANE Select	NP_000735.1:p.Thr614Met
ENST00000370263.9:c.1841C>T MANE Select	ENSP00000359285.4:p.Thr614Met
NM_000744.6:c.1841C>T	NP_000735.1:p.Thr614Met
NM_001256573.1:c.1313C>T	NP_001243502.1:p.Thr438Met
NM_001256573.2:c.1313C>T	NP_001243502.1:p.Thr438Met
NR_046317.1:n.2097C>T
NR_046317.2:n.2050C>T
ENST00000370263.8:c.1841C>T	ENSP00000359285.4:p.Thr614Met
ENST00000463705.5:n.2489C>T
ENST00000467563.3:n.1911C>T
ENST00000498043.6:c.1865C>T
ENST00000615287.4:c.1628C>T	ENSP00000483388.1:p.Thr543Met
ENST00000627000.1:c.*1530C>T	ENSP00000486914.1:n.*1530C>T
ENST00000631289.1:n.155C>T
XM_011528524.1:c.1628C>T	XP_011526826.1:p.Thr543Met
XM_017027625.2:c.1313C>T	XP_016883114.1:p.Thr438Met
XM_024451822.1:c.1313C>T	XP_024307590.1:p.Thr438Met