Canonical Allele Identifier: CA7684612

Gene: CHRNA3

Linked Data

• dbSNP Id: rs776121759
• ExAC: 15:78911159 TGACTGGGTCAGACACGTTGGCTACAG / T
• gnomAD v2: 15-78911159-TGACTGGGTCAGACACGTTGGCTACAG-T
• gnomAD v3: 15-78618817-TGACTGGGTCAGACACGTTGGCTACAG-T
• gnomAD v4: 15-78618817-TGACTGGGTCAGACACGTTGGCTACAG-T
• MyVariant Identifiers: chr15:g.78911160_78911185del (hg19) ; chr15:g.78618818_78618843del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78618819_78618844del , CM000677.2:g.78618819_78618844del	GRCh38
NC_000015.9:g.78911161_78911186del , CM000677.1:g.78911161_78911186del	GRCh37
NC_000015.8:g.76698216_76698241del	NCBI36
NG_016143.1:g.7453_7478del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.155_180del MANE Select	ENSP00000315602.5:p.Pro52HisfsTer16
ENST00000326828.5:c.155_180del	ENSP00000315602.5:p.Pro52HisfsTer16
ENST00000348639.7:c.155_180del	ENSP00000267951.4:p.Pro52HisfsTer16
ENST00000559080.1:c.-47_-22del	ENSP00000453993.1:n.-47_-22del
ENST00000559658.5:c.155_180del	ENSP00000452896.1:p.Pro52HisfsTer16
ENST00000561128.1:n.150_175del
NM_000743.4:c.155_180del	NP_000734.2:p.Pro52HisfsTer16
NM_001166694.1:c.155_180del	NP_001160166.1:p.Pro52HisfsTer16
NR_046313.1:n.656_681del
XM_006720382.1:c.-47_-22del	XP_006720445.1:n.-47_-22del
XM_011521173.1:c.74_99del	XP_011519475.1:p.Pro25HisfsTer16
XM_006720382.3:c.-47_-22del	XP_006720445.1:n.-47_-22del
NM_000743.5:c.155_180del MANE Select	NP_000734.2:p.Pro52HisfsTer16
NM_001166694.2:c.155_180del	NP_001160166.1:p.Pro52HisfsTer16
NR_046313.2:n.357_382del