Canonical Allele Identifier: CA2189599106

Gene: CHRNA3

Linked Data

• dbSNP Id: rs2053101502

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595991dup , CM000677.2:g.78595991dup	GRCh38
NC_000015.9:g.78888333dup , CM000677.1:g.78888333dup	GRCh37
NC_000015.8:g.76675388dup	NCBI36
NG_016143.1:g.30306dup
NG_023328.1:g.35472dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.*614dup MANE Select	ENSP00000315602.5:n.*614dup
ENST00000326828.5:c.*614dup	ENSP00000315602.5:n.*614dup
ENST00000348639.7:c.1390-2799dup	ENSP00000267951.4:n.1390-2799dup
ENST00000559002.5:n.193+550dup
ENST00000559658.5:c.*64+550dup	ENSP00000452896.1:n.*64+550dup
NM_000743.4:c.*614dup	NP_000734.2:n.*614dup
NM_001166694.1:c.1390-2799dup	NP_001160166.1:n.1390-2799dup
NR_046313.1:n.2083+550dup
XM_006720382.1:c.*614dup	XP_006720445.1:n.*614dup
XM_011521173.1:c.*614dup	XP_011519475.1:n.*614dup
XM_006720382.3:c.*614dup	XP_006720445.1:n.*614dup
NM_000743.5:c.*614dup MANE Select	NP_000734.2:n.*614dup
NM_001166694.2:c.1390-2799dup	NP_001160166.1:n.1390-2799dup
NR_046313.2:n.1784+550dup