Canonical Allele Identifier: CA2629785995
Gene: CHRNA5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78586771_78586778del , CM000677.2:g.78586771_78586778del GRCh38
NC_000015.9:g.78879113_78879120del , CM000677.1:g.78879113_78879120del GRCh37
NC_000015.8:g.76666168_76666175del NCBI36
NG_023328.1:g.26252_26259del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299565.9:c.303+82_303+89del MANE Select ENSP00000299565.5:n.303+82_303+89del
ENST00000394802.4:c.118+82_118+89del
ENST00000559554.5:c.303+82_303+89del ENSP00000453519.1:n.303+82_303+89del
NM_000745.3:c.303+82_303+89del NP_000736.2:n.303+82_303+89del
NM_001307945.1:c.303+82_303+89del NP_001294874.1:n.303+82_303+89del
XM_005254142.2:c.303+82_303+89del XP_005254199.1:n.303+82_303+89del
NM_001307945.2:c.303+82_303+89del NP_001294874.1:n.303+82_303+89del
NM_000745.4:c.303+82_303+89del MANE Select NP_000736.2:n.303+82_303+89del
NM_001395171.1:c.303+82_303+89del NP_001382100.1:n.303+82_303+89del
NM_001395172.1:c.303+82_303+89del NP_001382101.1:n.303+82_303+89del
NM_001395173.1:c.303+82_303+89del NP_001382102.1:n.303+82_303+89del
NM_001395174.1:c.303+82_303+89del NP_001382103.1:n.303+82_303+89del
NM_001395175.1:c.300+82_300+89del NP_001382104.1:n.300+82_300+89del