Canonical Allele Identifier: CA2629789155

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78602187-GGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602189_78602190del , CM000677.2:g.78602189_78602190del	GRCh38
NC_000015.9:g.78894531_78894532del , CM000677.1:g.78894531_78894532del	GRCh37
NC_000015.8:g.76681586_76681587del	NCBI36
NG_016143.1:g.24107_24108del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.453_454del MANE Select	ENSP00000315602.5:p.Pro152GlyfsTer4
ENST00000326828.5:c.453_454del	ENSP00000315602.5:p.Pro152GlyfsTer4
ENST00000348639.7:c.453_454del	ENSP00000267951.4:p.Pro152GlyfsTer4
ENST00000558903.1:n.160_161del
ENST00000559658.5:c.453_454del	ENSP00000452896.1:p.Pro152GlyfsTer4
NM_000743.4:c.453_454del	NP_000734.2:p.Pro152GlyfsTer4
NM_001166694.1:c.453_454del	NP_001160166.1:p.Pro152GlyfsTer4
NR_046313.1:n.954_955del
XM_006720382.1:c.252_253del	XP_006720445.1:p.Pro85GlyfsTer4
XM_011521173.1:c.372_373del	XP_011519475.1:p.Pro125GlyfsTer4
XM_006720382.3:c.252_253del	XP_006720445.1:p.Pro85GlyfsTer4
NM_000743.5:c.453_454del MANE Select	NP_000734.2:p.Pro152GlyfsTer4
NM_001166694.2:c.453_454del	NP_001160166.1:p.Pro152GlyfsTer4
NR_046313.2:n.655_656del