Canonical Allele Identifier: CA2189593738

Gene: CHRNA5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78590593G= , CM000677.2:g.78590593G=	GRCh38
NC_000015.9:g.78882935G= , CM000677.1:g.78882935G=	GRCh37
NC_000015.8:g.76669990G=	NCBI36
NG_023328.1:g.30074G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000299565.9:c.1202G= MANE Select	ENSP00000299565.5:p.Arg401=
ENST00000394802.4:c.522+495G=
ENST00000559554.5:c.458+744G=	ENSP00000453519.1:n.458+744G=
ENST00000559576.1:c.145+87G=
NM_000745.3:c.1202G=	NP_000736.2:p.Arg401=
NM_001307945.1:c.458+744G=	NP_001294874.1:n.458+744G=
XM_005254142.2:c.707+495G=	XP_005254199.1:n.707+495G=
NM_001307945.2:c.458+744G=	NP_001294874.1:n.458+744G=
NM_000745.4:c.1202G= MANE Select	NP_000736.2:p.Arg401=
NM_001395171.1:c.1115+87G=	NP_001382100.1:n.1115+87G=
NM_001395172.1:c.591+611G=	NP_001382101.1:n.591+611G=
NM_001395173.1:c.713+489G=	NP_001382102.1:n.713+489G=
NM_001395174.1:c.707+495G=	NP_001382103.1:n.707+495G=
NM_001395175.1:c.455+744G=	NP_001382104.1:n.455+744G=