Canonical Allele Identifier: CA273914043

Gene: CHRNA3

Linked Data

• dbSNP Id: rs775966273
• gnomAD v3: 15-78615440-T-TG
• gnomAD v4: 15-78615440-T-TG
• MyVariant Identifiers: chr15:g.78907782_78907783insG (hg19) ; chr15:g.78615440_78615441insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78615442dup , CM000677.2:g.78615442dup	GRCh38
NC_000015.9:g.78907784dup , CM000677.1:g.78907784dup	GRCh37
NC_000015.8:g.76694839dup	NCBI36
NG_016143.1:g.10855dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.377+1583dup MANE Select	ENSP00000315602.5:n.377+1583dup
ENST00000326828.5:c.377+1583dup	ENSP00000315602.5:n.377+1583dup
ENST00000348639.7:c.377+1583dup	ENSP00000267951.4:n.377+1583dup
ENST00000559658.5:c.377+1583dup	ENSP00000452896.1:n.377+1583dup
NM_000743.4:c.377+1583dup	NP_000734.2:n.377+1583dup
NM_001166694.1:c.377+1583dup	NP_001160166.1:n.377+1583dup
NR_046313.1:n.878+1583dup
XM_006720382.1:c.176+1583dup	XP_006720445.1:n.176+1583dup
XM_011521173.1:c.296+1583dup	XP_011519475.1:n.296+1583dup
XM_006720382.3:c.176+1583dup	XP_006720445.1:n.176+1583dup
NM_000743.5:c.377+1583dup MANE Select	NP_000734.2:n.377+1583dup
NM_001166694.2:c.377+1583dup	NP_001160166.1:n.377+1583dup
NR_046313.2:n.579+1583dup