Canonical Allele Identifier: CA2189598099

Gene: CHRNA5 CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78594818G= , CM000677.2:g.78594818G=	GRCh38
NC_000015.9:g.78887160G= , CM000677.1:g.78887160G=	GRCh37
NC_000015.8:g.76674215G=	NCBI36
NG_016143.1:g.31478C=
NG_023328.1:g.34299G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299565.9:c.*1565G= (CHRNA5) MANE Select	ENSP00000299565.5:n.*1565G=
ENST00000348639.7:c.1390-1627C= (CHRNA3)	ENSP00000267951.4:n.1390-1627C=
ENST00000559002.5:n.194-1627C= (CHRNA3)
ENST00000559658.5:c.*65-807C= (CHRNA3)	ENSP00000452896.1:n.*65-807C=
NM_000745.3:c.*1565G= (CHRNA5)	NP_000736.2:n.*1565G=
NM_001166694.1:c.1390-1627C= (CHRNA3)	NP_001160166.1:n.1390-1627C=
NM_001307945.1:c.*1702G= (CHRNA5)	NP_001294874.1:n.*1702G=
NR_046313.1:n.2084-807C= (CHRNA3)
NM_001166694.2:c.1390-1627C= (CHRNA3)	NP_001160166.1:n.1390-1627C=
NM_001307945.2:c.*1702G= (CHRNA5)	NP_001294874.1:n.*1702G=
NR_046313.2:n.1785-807C= (CHRNA3)
NM_000745.4:c.*1565G= (CHRNA5) MANE Select	NP_000736.2:n.*1565G=
NM_001395171.1:c.*1702G= (CHRNA5)	NP_001382100.1:n.*1702G=
NM_001395172.1:c.*1565G= (CHRNA5)	NP_001382101.1:n.*1565G=
NM_001395173.1:c.*1702G= (CHRNA5)	NP_001382102.1:n.*1702G=
NM_001395174.1:c.*1702G= (CHRNA5)	NP_001382103.1:n.*1702G=
NM_001395175.1:c.*1702G= (CHRNA5)	NP_001382104.1:n.*1702G=