Canonical Allele Identifier: CA2374740611

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63346204G= , CM000682.2:g.63346204G=	GRCh38
NC_000020.10:g.61977556G= , CM000682.1:g.61977556G=	GRCh37
NC_000020.9:g.61448000G=	NCBI36
NG_011931.1:g.20140C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000744.7:c.*534C= MANE Select	NP_000735.1:n.*534C=
ENST00000370263.9:c.*534C= MANE Select	ENSP00000359285.4:n.*534C=
NM_000744.6:c.*534C=	NP_000735.1:n.*534C=
NM_001256573.1:c.*534C=	NP_001243502.1:n.*534C=
NM_001256573.2:c.*534C=	NP_001243502.1:n.*534C=
NR_046317.1:n.2674C=
NR_046317.2:n.2627C=
ENST00000370263.8:c.*534C=	ENSP00000359285.4:n.*534C=
ENST00000463705.5:n.3066C=
ENST00000615287.4:c.*534C=	ENSP00000483388.1:n.*534C=
ENST00000631289.1:n.732C=
XM_011528524.1:c.*534C=	XP_011526826.1:n.*534C=
XM_017027625.2:c.*534C=	XP_016883114.1:n.*534C=
XM_024451822.1:c.*534C=	XP_024307590.1:n.*534C=