Canonical Allele Identifier: CA2374741448

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63347748G= , CM000682.2:g.63347748G=	GRCh38
NC_000020.10:g.61979100G= , CM000682.1:g.61979100G=	GRCh37
NC_000020.9:g.61449544G=	NCBI36
NG_011931.1:g.18596C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000744.7:c.1759-885C= MANE Select	NP_000735.1:n.1759-885C=
ENST00000370263.9:c.1759-885C= MANE Select	ENSP00000359285.4:n.1759-885C=
NM_000744.6:c.1759-885C=	NP_000735.1:n.1759-885C=
NM_001256573.1:c.1231-885C=	NP_001243502.1:n.1231-885C=
NM_001256573.2:c.1231-885C=	NP_001243502.1:n.1231-885C=
NR_046317.1:n.2015-885C=
NR_046317.2:n.1968-885C=
ENST00000370263.8:c.1759-885C=	ENSP00000359285.4:n.1759-885C=
ENST00000463705.5:n.2407-885C=
ENST00000467563.3:n.1829-885C=
ENST00000498043.6:c.1783-885C=
ENST00000615287.4:c.1546-885C=	ENSP00000483388.1:n.1546-885C=
ENST00000627000.1:c.*1448-885C=	ENSP00000486914.1:n.*1448-885C=
XM_011528524.1:c.1546-885C=	XP_011526826.1:n.1546-885C=
XM_017027625.2:c.1231-885C=	XP_016883114.1:n.1231-885C=
XM_024451822.1:c.1231-885C=	XP_024307590.1:n.1231-885C=