Canonical Allele Identifier: CA2629789509

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78602380-G-GAGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602382_78602383insTTAG , CM000677.2:g.78602382_78602383insTTAG	GRCh38
NC_000015.9:g.78894724_78894725insTTAG , CM000677.1:g.78894724_78894725insTTAG	GRCh37
NC_000015.8:g.76681779_76681780insTTAG	NCBI36
NG_016143.1:g.23915_23916insAACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.378-117_378-116insAACT MANE Select	ENSP00000315602.5:n.378-117_378-116insAACT
ENST00000326828.5:c.378-117_378-116insAACT	ENSP00000315602.5:n.378-117_378-116insAACT
ENST00000348639.7:c.378-117_378-116insAACT	ENSP00000267951.4:n.378-117_378-116insAACT
ENST00000558903.1:n.85-117_85-116insAACT
ENST00000559658.5:c.378-117_378-116insAACT	ENSP00000452896.1:n.378-117_378-116insAACT
NM_000743.4:c.378-117_378-116insAACT	NP_000734.2:n.378-117_378-116insAACT
NM_001166694.1:c.378-117_378-116insAACT	NP_001160166.1:n.378-117_378-116insAACT
NR_046313.1:n.879-117_879-116insAACT
XM_006720382.1:c.177-117_177-116insAACT	XP_006720445.1:n.177-117_177-116insAACT
XM_011521173.1:c.297-117_297-116insAACT	XP_011519475.1:n.297-117_297-116insAACT
XM_006720382.3:c.177-117_177-116insAACT	XP_006720445.1:n.177-117_177-116insAACT
NM_000743.5:c.378-117_378-116insAACT MANE Select	NP_000734.2:n.378-117_378-116insAACT
NM_001166694.2:c.378-117_378-116insAACT	NP_001160166.1:n.378-117_378-116insAACT
NR_046313.2:n.580-117_580-116insAACT