Canonical Allele Identifier: CA2189599029

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595899G= , CM000677.2:g.78595899G=	GRCh38
NC_000015.9:g.78888241G= , CM000677.1:g.78888241G=	GRCh37
NC_000015.8:g.76675296G=	NCBI36
NG_016143.1:g.30397C=
NG_023328.1:g.35380G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.*705C= MANE Select	ENSP00000315602.5:n.*705C=
ENST00000326828.5:c.*705C=	ENSP00000315602.5:n.*705C=
ENST00000348639.7:c.1390-2708C=	ENSP00000267951.4:n.1390-2708C=
ENST00000559002.5:n.193+641C=
ENST00000559658.5:c.*64+641C=	ENSP00000452896.1:n.*64+641C=
NM_000743.4:c.*705C=	NP_000734.2:n.*705C=
NM_001166694.1:c.1390-2708C=	NP_001160166.1:n.1390-2708C=
NR_046313.1:n.2083+641C=
XM_006720382.1:c.*705C=	XP_006720445.1:n.*705C=
XM_011521173.1:c.*705C=	XP_011519475.1:n.*705C=
XM_006720382.3:c.*705C=	XP_006720445.1:n.*705C=
NM_000743.5:c.*705C= MANE Select	NP_000734.2:n.*705C=
NM_001166694.2:c.1390-2708C=	NP_001160166.1:n.1390-2708C=
NR_046313.2:n.1784+641C=