Canonical Allele Identifier: CA7684530

Gene: CHRNA3

Linked Data

• dbSNP Id: rs754945008
• ExAC: 15:78909393 C / CA
• gnomAD v2: 15-78909393-C-CA
• gnomAD v4: 15-78617051-C-CA
• MyVariant Identifiers: chr15:g.78909393_78909394insA (hg19) ; chr15:g.78617051_78617052insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78617052dup , CM000677.2:g.78617052dup	GRCh38
NC_000015.9:g.78909394dup , CM000677.1:g.78909394dup	GRCh37
NC_000015.8:g.76696449dup	NCBI36
NG_016143.1:g.9244dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.349dup MANE Select	ENSP00000315602.5:p.Trp117LeufsTer9
ENST00000326828.5:c.349dup	ENSP00000315602.5:p.Trp117LeufsTer9
ENST00000348639.7:c.349dup	ENSP00000267951.4:p.Trp117LeufsTer9
ENST00000559658.5:c.349dup	ENSP00000452896.1:p.Trp117LeufsTer9
NM_000743.4:c.349dup	NP_000734.2:p.Trp117LeufsTer9
NM_001166694.1:c.349dup	NP_001160166.1:p.Trp117LeufsTer9
NR_046313.1:n.850dup
XM_006720382.1:c.148dup	XP_006720445.1:p.Trp50LeufsTer9
XM_011521173.1:c.268dup	XP_011519475.1:p.Trp90LeufsTer9
XM_006720382.3:c.148dup	XP_006720445.1:p.Trp50LeufsTer9
NM_000743.5:c.349dup MANE Select	NP_000734.2:p.Trp117LeufsTer9
NM_001166694.2:c.349dup	NP_001160166.1:p.Trp117LeufsTer9
NR_046313.2:n.551dup