Canonical Allele Identifier: CA2629783016
Gene: CHRNA5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78565568del , CM000677.2:g.78565568del GRCh38
NC_000015.9:g.78857910del , CM000677.1:g.78857910del GRCh37
NC_000015.8:g.76644965del NCBI36
NG_023328.1:g.5049del

Transcript Alleles

HGVS Amino-acid change
ENST00000299565.9:c.-152del MANE Select ENSP00000299565.5:n.-152del
NM_000745.3:c.-152del NP_000736.2:n.-152del
NM_001307945.1:c.-152del NP_001294874.1:n.-152del
XM_005254142.2:c.-152del XP_005254199.1:n.-152del
NM_001307945.2:c.-152del NP_001294874.1:n.-152del
NM_000745.4:c.-152del MANE Select NP_000736.2:n.-152del
NM_001395171.1:c.-152del NP_001382100.1:n.-152del
NM_001395172.1:c.-152del NP_001382101.1:n.-152del
NM_001395173.1:c.-152del NP_001382102.1:n.-152del
NM_001395174.1:c.-152del NP_001382103.1:n.-152del
NM_001395175.1:c.-152del NP_001382104.1:n.-152del