Canonical Allele Identifier: CA715959588

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1420477629
• gnomAD v3: 15-78595886-G-GA
• gnomAD v4: 15-78595886-G-GA
• MyVariant Identifiers: chr15:g.78888228_78888229insA (hg19) ; chr15:g.78595886_78595887insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595888dup , CM000677.2:g.78595888dup	GRCh38
NC_000015.9:g.78888230dup , CM000677.1:g.78888230dup	GRCh37
NC_000015.8:g.76675285dup	NCBI36
NG_016143.1:g.30409dup
NG_023328.1:g.35369dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.*717dup MANE Select	ENSP00000315602.5:n.*717dup
ENST00000326828.5:c.*717dup	ENSP00000315602.5:n.*717dup
ENST00000348639.7:c.1390-2696dup	ENSP00000267951.4:n.1390-2696dup
ENST00000559002.5:n.193+653dup
ENST00000559658.5:c.*64+653dup	ENSP00000452896.1:n.*64+653dup
NM_000743.4:c.*717dup	NP_000734.2:n.*717dup
NM_001166694.1:c.1390-2696dup	NP_001160166.1:n.1390-2696dup
NR_046313.1:n.2083+653dup
XM_006720382.1:c.*717dup	XP_006720445.1:n.*717dup
XM_011521173.1:c.*717dup	XP_011519475.1:n.*717dup
XM_006720382.3:c.*717dup	XP_006720445.1:n.*717dup
NM_000743.5:c.*717dup MANE Select	NP_000734.2:n.*717dup
NM_001166694.2:c.1390-2696dup	NP_001160166.1:n.1390-2696dup
NR_046313.2:n.1784+653dup