Canonical Allele Identifier: CA2629793129

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78595858-T-TCC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595860_78595861dup , CM000677.2:g.78595860_78595861dup	GRCh38
NC_000015.9:g.78888202_78888203dup , CM000677.1:g.78888202_78888203dup	GRCh37
NC_000015.8:g.76675257_76675258dup	NCBI36
NG_016143.1:g.30436_30437dup
NG_023328.1:g.35341_35342dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.*744_*745dup MANE Select	ENSP00000315602.5:n.*744_*745dup
ENST00000326828.5:c.*744_*745dup	ENSP00000315602.5:n.*744_*745dup
ENST00000348639.7:c.1390-2669_1390-2668dup	ENSP00000267951.4:n.1390-2669_1390-2668dup
ENST00000559002.5:n.193+680_193+681dup
ENST00000559658.5:c.*64+680_*64+681dup	ENSP00000452896.1:n.*64+680_*64+681dup
NM_000743.4:c.*744_*745dup	NP_000734.2:n.*744_*745dup
NM_001166694.1:c.1390-2669_1390-2668dup	NP_001160166.1:n.1390-2669_1390-2668dup
NR_046313.1:n.2083+680_2083+681dup
XM_006720382.1:c.*744_*745dup	XP_006720445.1:n.*744_*745dup
XM_011521173.1:c.*744_*745dup	XP_011519475.1:n.*744_*745dup
XM_006720382.3:c.*744_*745dup	XP_006720445.1:n.*744_*745dup
NM_000743.5:c.*744_*745dup MANE Select	NP_000734.2:n.*744_*745dup
NM_001166694.2:c.1390-2669_1390-2668dup	NP_001160166.1:n.1390-2669_1390-2668dup
NR_046313.2:n.1784+680_1784+681dup