Canonical Allele Identifier: CA2374743224

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350905G= , CM000682.2:g.63350905G=	GRCh38
NC_000020.10:g.61982257G= , CM000682.1:g.61982257G=	GRCh37
NC_000020.9:g.61452701G=	NCBI36
NG_011931.1:g.15439C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.506C= MANE Select	ENSP00000359285.4:p.Pro169=
ENST00000370263.8:c.506C=	ENSP00000359285.4:p.Pro169=
ENST00000463705.5:n.1154C=
ENST00000467563.3:n.576C=
ENST00000498043.6:c.530C=
ENST00000615287.4:c.293C=	ENSP00000483388.1:p.Pro98=
ENST00000627000.1:c.*195C=	ENSP00000486914.1:n.*195C=
ENST00000630240.1:n.227C=
NM_000744.6:c.506C=	NP_000735.1:p.Pro169=
NM_001256573.1:c.-23C=	NP_001243502.1:n.-23C=
NR_046317.1:n.762C=
XM_011528524.1:c.293C=	XP_011526826.1:p.Pro98=
XM_017027625.2:c.-23C=	XP_016883114.1:n.-23C=
XM_024451822.1:c.-23C=	XP_024307590.1:n.-23C=
NM_001256573.2:c.-23C=	NP_001243502.1:n.-23C=
NR_046317.2:n.715C=
NM_000744.7:c.506C= MANE Select	NP_000735.1:p.Pro169=