Canonical Allele Identifier: CA971779445

Gene: CHRNA3

Linked Data

• dbSNP Id: rs2053104050
• gnomAD v3: 15-78596061-A-ATAAT
• gnomAD v4: 15-78596061-A-ATAAT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78596063_78596066dup , CM000677.2:g.78596063_78596066dup	GRCh38
NC_000015.9:g.78888405_78888408dup , CM000677.1:g.78888405_78888408dup	GRCh37
NC_000015.8:g.76675460_76675463dup	NCBI36
NG_016143.1:g.30231_30234dup
NG_023328.1:g.35544_35547dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.*539_*542dup MANE Select	ENSP00000315602.5:n.*539_*542dup
ENST00000326828.5:c.*539_*542dup	ENSP00000315602.5:n.*539_*542dup
ENST00000348639.7:c.1390-2874_1390-2871dup	ENSP00000267951.4:n.1390-2874_1390-2871dup
ENST00000559002.5:n.193+475_193+478dup
ENST00000559658.5:c.*64+475_*64+478dup	ENSP00000452896.1:n.*64+475_*64+478dup
NM_000743.4:c.*539_*542dup	NP_000734.2:n.*539_*542dup
NM_001166694.1:c.1390-2874_1390-2871dup	NP_001160166.1:n.1390-2874_1390-2871dup
NR_046313.1:n.2083+475_2083+478dup
XM_006720382.1:c.*539_*542dup	XP_006720445.1:n.*539_*542dup
XM_011521173.1:c.*539_*542dup	XP_011519475.1:n.*539_*542dup
XM_006720382.3:c.*539_*542dup	XP_006720445.1:n.*539_*542dup
NM_000743.5:c.*539_*542dup MANE Select	NP_000734.2:n.*539_*542dup
NM_001166694.2:c.1390-2874_1390-2871dup	NP_001160166.1:n.1390-2874_1390-2871dup
NR_046313.2:n.1784+475_1784+478dup