Canonical Allele Identifier: CA919597465

Gene: CHRNA3

Linked Data

• dbSNP Id: rs375922184

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595896delinsCCC , CM000677.2:g.78595896delinsCCC	GRCh38
NC_000015.9:g.78888238delinsCCC , CM000677.1:g.78888238delinsCCC	GRCh37
NC_000015.8:g.76675293delinsCCC	NCBI36
NG_016143.1:g.30400delinsGGG
NG_023328.1:g.35377delinsCCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.*708delinsGGG MANE Select	ENSP00000315602.5:n.*708delinsGGG
ENST00000326828.5:c.*708delinsGGG	ENSP00000315602.5:n.*708delinsGGG
ENST00000348639.7:c.1390-2705delinsGGG	ENSP00000267951.4:n.1390-2705delinsGGG
ENST00000559002.5:n.193+644delinsGGG
ENST00000559658.5:c.*64+644delinsGGG	ENSP00000452896.1:n.*64+644delinsGGG
NM_000743.4:c.*708delinsGGG	NP_000734.2:n.*708delinsGGG
NM_001166694.1:c.1390-2705delinsGGG	NP_001160166.1:n.1390-2705delinsGGG
NR_046313.1:n.2083+644delinsGGG
XM_006720382.1:c.*708delinsGGG	XP_006720445.1:n.*708delinsGGG
XM_011521173.1:c.*708delinsGGG	XP_011519475.1:n.*708delinsGGG
XM_006720382.3:c.*708delinsGGG	XP_006720445.1:n.*708delinsGGG
NM_000743.5:c.*708delinsGGG MANE Select	NP_000734.2:n.*708delinsGGG
NM_001166694.2:c.1390-2705delinsGGG	NP_001160166.1:n.1390-2705delinsGGG
NR_046313.2:n.1784+644delinsGGG