Canonical Allele Identifier: CA2189588230

Gene: CHRNA5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78586134A= , CM000677.2:g.78586134A=	GRCh38
NC_000015.9:g.78878476A= , CM000677.1:g.78878476A=	GRCh37
NC_000015.8:g.76665531A=	NCBI36
NG_023328.1:g.25615A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000299565.9:c.259-511A= MANE Select	ENSP00000299565.5:n.259-511A=
ENST00000394802.4:c.74-511A=
ENST00000559554.5:c.259-511A=	ENSP00000453519.1:n.259-511A=
NM_000745.3:c.259-511A=	NP_000736.2:n.259-511A=
NM_001307945.1:c.259-511A=	NP_001294874.1:n.259-511A=
XM_005254142.2:c.259-511A=	XP_005254199.1:n.259-511A=
NM_001307945.2:c.259-511A=	NP_001294874.1:n.259-511A=
NM_000745.4:c.259-511A= MANE Select	NP_000736.2:n.259-511A=
NM_001395171.1:c.259-511A=	NP_001382100.1:n.259-511A=
NM_001395172.1:c.259-511A=	NP_001382101.1:n.259-511A=
NM_001395173.1:c.259-511A=	NP_001382102.1:n.259-511A=
NM_001395174.1:c.259-511A=	NP_001382103.1:n.259-511A=
NM_001395175.1:c.256-511A=	NP_001382104.1:n.256-511A=