Canonical Allele Identifier: CA619238127

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1355371311
• gnomAD v2: 15-78907837-C-CT
• gnomAD v3: 15-78615495-C-CT
• gnomAD v4: 15-78615495-C-CT
• MyVariant Identifiers: chr15:g.78907837_78907838insT (hg19) ; chr15:g.78615495_78615496insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78615496dup , CM000677.2:g.78615496dup	GRCh38
NC_000015.9:g.78907838dup , CM000677.1:g.78907838dup	GRCh37
NC_000015.8:g.76694893dup	NCBI36
NG_016143.1:g.10800dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.377+1528dup MANE Select	ENSP00000315602.5:n.377+1528dup
ENST00000326828.5:c.377+1528dup	ENSP00000315602.5:n.377+1528dup
ENST00000348639.7:c.377+1528dup	ENSP00000267951.4:n.377+1528dup
ENST00000559658.5:c.377+1528dup	ENSP00000452896.1:n.377+1528dup
NM_000743.4:c.377+1528dup	NP_000734.2:n.377+1528dup
NM_001166694.1:c.377+1528dup	NP_001160166.1:n.377+1528dup
NR_046313.1:n.878+1528dup
XM_006720382.1:c.176+1528dup	XP_006720445.1:n.176+1528dup
XM_011521173.1:c.296+1528dup	XP_011519475.1:n.296+1528dup
XM_006720382.3:c.176+1528dup	XP_006720445.1:n.176+1528dup
NM_000743.5:c.377+1528dup MANE Select	NP_000734.2:n.377+1528dup
NM_001166694.2:c.377+1528dup	NP_001160166.1:n.377+1528dup
NR_046313.2:n.579+1528dup