Canonical Allele Identifier: CA2189591051

Gene: CHRNA5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78588993_78588997delinsTTGTC , CM000677.2:g.78588993_78588997delinsTTGTC	GRCh38
NC_000015.9:g.78881335_78881339delinsTTGTC , CM000677.1:g.78881335_78881339delinsTTGTC	GRCh37
NC_000015.8:g.76668390_76668394delinsTTGTC	NCBI36
NG_023328.1:g.28474_28478delinsTTGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299565.9:c.413+570_413+574delinsTTGTC MANE Select	ENSP00000299565.5:n.413+570_413+574delinsTTGTC
ENST00000394802.4:c.228+570_228+574delinsTTGTC
ENST00000559554.5:c.413+570_413+574delinsTTGTC	ENSP00000453519.1:n.413+570_413+574delinsTTGTC
NM_000745.3:c.413+570_413+574delinsTTGTC	NP_000736.2:n.413+570_413+574delinsTTGTC
NM_001307945.1:c.413+570_413+574delinsTTGTC	NP_001294874.1:n.413+570_413+574delinsTTGTC
XM_005254142.2:c.413+570_413+574delinsTTGTC	XP_005254199.1:n.413+570_413+574delinsTTGTC
NM_001307945.2:c.413+570_413+574delinsTTGTC	NP_001294874.1:n.413+570_413+574delinsTTGTC
NM_000745.4:c.413+570_413+574delinsTTGTC MANE Select	NP_000736.2:n.413+570_413+574delinsTTGTC
NM_001395171.1:c.413+570_413+574delinsTTGTC	NP_001382100.1:n.413+570_413+574delinsTTGTC
NM_001395172.1:c.413+570_413+574delinsTTGTC	NP_001382101.1:n.413+570_413+574delinsTTGTC
NM_001395173.1:c.413+570_413+574delinsTTGTC	NP_001382102.1:n.413+570_413+574delinsTTGTC
NM_001395174.1:c.413+570_413+574delinsTTGTC	NP_001382103.1:n.413+570_413+574delinsTTGTC
NM_001395175.1:c.410+570_410+574delinsTTGTC	NP_001382104.1:n.410+570_410+574delinsTTGTC