Canonical Allele Identifier: CA971782800

Gene: CHRNA3

Linked Data

• dbSNP Id: rs2053208862
• gnomAD v3: 15-78601933-TGTA-T
• gnomAD v4: 15-78601933-TGTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601934_78601936del , CM000677.2:g.78601934_78601936del	GRCh38
NC_000015.9:g.78894276_78894278del , CM000677.1:g.78894276_78894278del	GRCh37
NC_000015.8:g.76681331_76681333del	NCBI36
NG_016143.1:g.24360_24362del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.706_708del MANE Select	ENSP00000315602.5:p.Tyr236del
ENST00000326828.5:c.706_708del	ENSP00000315602.5:p.Tyr236del
ENST00000348639.7:c.706_708del	ENSP00000267951.4:p.Tyr236del
ENST00000558903.1:n.413_415del
ENST00000559658.5:c.706_708del	ENSP00000452896.1:p.Tyr236del
NM_000743.4:c.706_708del	NP_000734.2:p.Tyr236del
NM_001166694.1:c.706_708del	NP_001160166.1:p.Tyr236del
NR_046313.1:n.1207_1209del
XM_006720382.1:c.505_507del	XP_006720445.1:p.Tyr169del
XM_011521173.1:c.625_627del	XP_011519475.1:p.Tyr209del
XM_006720382.3:c.505_507del	XP_006720445.1:p.Tyr169del
NM_000743.5:c.706_708del MANE Select	NP_000734.2:p.Tyr236del
NM_001166694.2:c.706_708del	NP_001160166.1:p.Tyr236del
NR_046313.2:n.908_910del