Canonical Allele Identifier: CA619238130

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1362941721
• gnomAD v2: 15-78907940-ACC-A
• gnomAD v3: 15-78615598-ACC-A
• gnomAD v4: 15-78615598-ACC-A
• MyVariant Identifiers: chr15:g.78907941_78907942del (hg19) ; chr15:g.78615599_78615600del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78615600_78615601del , CM000677.2:g.78615600_78615601del	GRCh38
NC_000015.9:g.78907942_78907943del , CM000677.1:g.78907942_78907943del	GRCh37
NC_000015.8:g.76694997_76694998del	NCBI36
NG_016143.1:g.10696_10697del

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.377+1424_377+1425del MANE Select	ENSP00000315602.5:n.377+1424_377+1425del
ENST00000326828.5:c.377+1424_377+1425del	ENSP00000315602.5:n.377+1424_377+1425del
ENST00000348639.7:c.377+1424_377+1425del	ENSP00000267951.4:n.377+1424_377+1425del
ENST00000559658.5:c.377+1424_377+1425del	ENSP00000452896.1:n.377+1424_377+1425del
NM_000743.4:c.377+1424_377+1425del	NP_000734.2:n.377+1424_377+1425del
NM_001166694.1:c.377+1424_377+1425del	NP_001160166.1:n.377+1424_377+1425del
NR_046313.1:n.878+1424_878+1425del
XM_006720382.1:c.176+1424_176+1425del	XP_006720445.1:n.176+1424_176+1425del
XM_011521173.1:c.296+1424_296+1425del	XP_011519475.1:n.296+1424_296+1425del
XM_006720382.3:c.176+1424_176+1425del	XP_006720445.1:n.176+1424_176+1425del
NM_000743.5:c.377+1424_377+1425del MANE Select	NP_000734.2:n.377+1424_377+1425del
NM_001166694.2:c.377+1424_377+1425del	NP_001160166.1:n.377+1424_377+1425del
NR_046313.2:n.579+1424_579+1425del