Canonical Allele Identifier: CA273893236

Gene: CHRNA5

Linked Data

• dbSNP Id: rs979733074
• MyVariant Identifiers: chr15:g.78879238_78879240del (hg19) ; chr15:g.78586896_78586898del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78586897_78586899del , CM000677.2:g.78586897_78586899del	GRCh38
NC_000015.9:g.78879239_78879241del , CM000677.1:g.78879239_78879241del	GRCh37
NC_000015.8:g.76666294_76666296del	NCBI36
NG_023328.1:g.26378_26380del

Transcript Alleles

HGVS	Amino-acid change
ENST00000299565.9:c.303+208_303+210del MANE Select	ENSP00000299565.5:n.303+208_303+210del
ENST00000394802.4:c.118+208_118+210del
ENST00000559554.5:c.303+208_303+210del	ENSP00000453519.1:n.303+208_303+210del
NM_000745.3:c.303+208_303+210del	NP_000736.2:n.303+208_303+210del
NM_001307945.1:c.303+208_303+210del	NP_001294874.1:n.303+208_303+210del
XM_005254142.2:c.303+208_303+210del	XP_005254199.1:n.303+208_303+210del
NM_001307945.2:c.303+208_303+210del	NP_001294874.1:n.303+208_303+210del
NM_000745.4:c.303+208_303+210del MANE Select	NP_000736.2:n.303+208_303+210del
NM_001395171.1:c.303+208_303+210del	NP_001382100.1:n.303+208_303+210del
NM_001395172.1:c.303+208_303+210del	NP_001382101.1:n.303+208_303+210del
NM_001395173.1:c.303+208_303+210del	NP_001382102.1:n.303+208_303+210del
NM_001395174.1:c.303+208_303+210del	NP_001382103.1:n.303+208_303+210del
NM_001395175.1:c.300+208_300+210del	NP_001382104.1:n.300+208_300+210del