Canonical Allele Identifier: CA2629788517
Gene: CHRNA5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78589425_78589426insATGG , CM000677.2:g.78589425_78589426insATGG GRCh38
NC_000015.9:g.78881767_78881768insATGG , CM000677.1:g.78881767_78881768insATGG GRCh37
NC_000015.8:g.76668822_76668823insATGG NCBI36
NG_023328.1:g.28906_28907insATGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000299565.9:c.414-380_414-379insATGG MANE Select ENSP00000299565.5:n.414-380_414-379insATGG
ENST00000394802.4:c.229-380_229-379insATGG
ENST00000559554.5:c.414-380_414-379insATGG ENSP00000453519.1:n.414-380_414-379insATGG
NM_000745.3:c.414-380_414-379insATGG NP_000736.2:n.414-380_414-379insATGG
NM_001307945.1:c.414-380_414-379insATGG NP_001294874.1:n.414-380_414-379insATGG
XM_005254142.2:c.414-380_414-379insATGG XP_005254199.1:n.414-380_414-379insATGG
NM_001307945.2:c.414-380_414-379insATGG NP_001294874.1:n.414-380_414-379insATGG
NM_000745.4:c.414-380_414-379insATGG MANE Select NP_000736.2:n.414-380_414-379insATGG
NM_001395171.1:c.414-380_414-379insATGG NP_001382100.1:n.414-380_414-379insATGG
NM_001395172.1:c.414-380_414-379insATGG NP_001382101.1:n.414-380_414-379insATGG
NM_001395173.1:c.414-380_414-379insATGG NP_001382102.1:n.414-380_414-379insATGG
NM_001395174.1:c.414-380_414-379insATGG NP_001382103.1:n.414-380_414-379insATGG
NM_001395175.1:c.411-380_411-379insATGG NP_001382104.1:n.411-380_411-379insATGG