Canonical Allele Identifier: CA715973560

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1335752313
• gnomAD v3: 15-78615734-CCTGTA-C
• gnomAD v4: 15-78615734-CCTGTA-C
• MyVariant Identifiers: chr15:g.78908077_78908081del (hg19) ; chr15:g.78615735_78615739del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78615735_78615739del , CM000677.2:g.78615735_78615739del	GRCh38
NC_000015.9:g.78908077_78908081del , CM000677.1:g.78908077_78908081del	GRCh37
NC_000015.8:g.76695132_76695136del	NCBI36
NG_016143.1:g.10557_10561del

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.377+1285_377+1289del MANE Select	ENSP00000315602.5:n.377+1285_377+1289del
ENST00000326828.5:c.377+1285_377+1289del	ENSP00000315602.5:n.377+1285_377+1289del
ENST00000348639.7:c.377+1285_377+1289del	ENSP00000267951.4:n.377+1285_377+1289del
ENST00000559658.5:c.377+1285_377+1289del	ENSP00000452896.1:n.377+1285_377+1289del
NM_000743.4:c.377+1285_377+1289del	NP_000734.2:n.377+1285_377+1289del
NM_001166694.1:c.377+1285_377+1289del	NP_001160166.1:n.377+1285_377+1289del
NR_046313.1:n.878+1285_878+1289del
XM_006720382.1:c.176+1285_176+1289del	XP_006720445.1:n.176+1285_176+1289del
XM_011521173.1:c.296+1285_296+1289del	XP_011519475.1:n.296+1285_296+1289del
XM_006720382.3:c.176+1285_176+1289del	XP_006720445.1:n.176+1285_176+1289del
NM_000743.5:c.377+1285_377+1289del MANE Select	NP_000734.2:n.377+1285_377+1289del
NM_001166694.2:c.377+1285_377+1289del	NP_001160166.1:n.377+1285_377+1289del
NR_046313.2:n.579+1285_579+1289del