Canonical Allele Identifier: CA2374742505

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349661_63349663delinsCTG , CM000682.2:g.63349661_63349663delinsCTG	GRCh38
NC_000020.10:g.61981013_61981015delinsCTG , CM000682.1:g.61981013_61981015delinsCTG	GRCh37
NC_000020.9:g.61451457_61451459delinsCTG	NCBI36
NG_011931.1:g.16681_16683delinsCAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000370263.9:c.1748_1750delinsCAG MANE Select	ENSP00000359285.4:p.Thr583=
ENST00000370263.8:c.1748_1750delinsCAG	ENSP00000359285.4:p.Thr583=
ENST00000463705.5:n.2396_2398delinsCAG
ENST00000467563.3:n.1818_1820delinsCAG
ENST00000498043.6:c.1772_1774delinsCAG
ENST00000615287.4:c.1535_1537delinsCAG	ENSP00000483388.1:p.Thr512=
ENST00000627000.1:c.*1437_*1439delinsCAG	ENSP00000486914.1:n.*1437_*1439delinsCAG
ENST00000630240.1:n.1469_1471delinsCAG
NM_000744.6:c.1748_1750delinsCAG	NP_000735.1:p.Thr583=
NM_001256573.1:c.1220_1222delinsCAG	NP_001243502.1:p.Thr407=
NR_046317.1:n.2004_2006delinsCAG
XM_011528524.1:c.1535_1537delinsCAG	XP_011526826.1:p.Thr512=
XM_017027625.2:c.1220_1222delinsCAG	XP_016883114.1:p.Thr407=
XM_024451822.1:c.1220_1222delinsCAG	XP_024307590.1:p.Thr407=
NM_001256573.2:c.1220_1222delinsCAG	NP_001243502.1:p.Thr407=
NR_046317.2:n.1957_1959delinsCAG
NM_000744.7:c.1748_1750delinsCAG MANE Select	NP_000735.1:p.Thr583=