Canonical Allele Identifier: CA2189591152
Gene: CHRNA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78589093_78589094delinsGA , CM000677.2:g.78589093_78589094delinsGA GRCh38
NC_000015.9:g.78881435_78881436delinsGA , CM000677.1:g.78881435_78881436delinsGA GRCh37
NC_000015.8:g.76668490_76668491delinsGA NCBI36
NG_023328.1:g.28574_28575delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000299565.9:c.413+670_413+671delinsGA MANE Select ENSP00000299565.5:n.413+670_413+671delinsGA
ENST00000394802.4:c.228+670_228+671delinsGA
ENST00000559554.5:c.413+670_413+671delinsGA ENSP00000453519.1:n.413+670_413+671delinsGA
NM_000745.3:c.413+670_413+671delinsGA NP_000736.2:n.413+670_413+671delinsGA
NM_001307945.1:c.413+670_413+671delinsGA NP_001294874.1:n.413+670_413+671delinsGA
XM_005254142.2:c.413+670_413+671delinsGA XP_005254199.1:n.413+670_413+671delinsGA
NM_001307945.2:c.413+670_413+671delinsGA NP_001294874.1:n.413+670_413+671delinsGA
NM_000745.4:c.413+670_413+671delinsGA MANE Select NP_000736.2:n.413+670_413+671delinsGA
NM_001395171.1:c.413+670_413+671delinsGA NP_001382100.1:n.413+670_413+671delinsGA
NM_001395172.1:c.413+670_413+671delinsGA NP_001382101.1:n.413+670_413+671delinsGA
NM_001395173.1:c.413+670_413+671delinsGA NP_001382102.1:n.413+670_413+671delinsGA
NM_001395174.1:c.413+670_413+671delinsGA NP_001382103.1:n.413+670_413+671delinsGA
NM_001395175.1:c.410+670_410+671delinsGA NP_001382104.1:n.410+670_410+671delinsGA