Canonical Allele Identifier: CA2189591970

Gene: CHRNA5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78589453G= , CM000677.2:g.78589453G=	GRCh38
NC_000015.9:g.78881795G= , CM000677.1:g.78881795G=	GRCh37
NC_000015.8:g.76668850G=	NCBI36
NG_023328.1:g.28934G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299565.9:c.414-352G= MANE Select	ENSP00000299565.5:n.414-352G=
ENST00000394802.4:c.229-352G=
ENST00000559554.5:c.414-352G=	ENSP00000453519.1:n.414-352G=
NM_000745.3:c.414-352G=	NP_000736.2:n.414-352G=
NM_001307945.1:c.414-352G=	NP_001294874.1:n.414-352G=
XM_005254142.2:c.414-352G=	XP_005254199.1:n.414-352G=
NM_001307945.2:c.414-352G=	NP_001294874.1:n.414-352G=
NM_000745.4:c.414-352G= MANE Select	NP_000736.2:n.414-352G=
NM_001395171.1:c.414-352G=	NP_001382100.1:n.414-352G=
NM_001395172.1:c.414-352G=	NP_001382101.1:n.414-352G=
NM_001395173.1:c.414-352G=	NP_001382102.1:n.414-352G=
NM_001395174.1:c.414-352G=	NP_001382103.1:n.414-352G=
NM_001395175.1:c.411-352G=	NP_001382104.1:n.411-352G=