Canonical Allele Identifier: CA715973501

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1478214507
• gnomAD v3: 15-78615671-A-AAT
• gnomAD v4: 15-78615671-A-AAT
• MyVariant Identifiers: chr15:g.78908013_78908014insAT (hg19) ; chr15:g.78615671_78615672insAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78615673_78615674dup , CM000677.2:g.78615673_78615674dup	GRCh38
NC_000015.9:g.78908015_78908016dup , CM000677.1:g.78908015_78908016dup	GRCh37
NC_000015.8:g.76695070_76695071dup	NCBI36
NG_016143.1:g.10623_10624dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.377+1351_377+1352dup MANE Select	ENSP00000315602.5:n.377+1351_377+1352dup
ENST00000326828.5:c.377+1351_377+1352dup	ENSP00000315602.5:n.377+1351_377+1352dup
ENST00000348639.7:c.377+1351_377+1352dup	ENSP00000267951.4:n.377+1351_377+1352dup
ENST00000559658.5:c.377+1351_377+1352dup	ENSP00000452896.1:n.377+1351_377+1352dup
NM_000743.4:c.377+1351_377+1352dup	NP_000734.2:n.377+1351_377+1352dup
NM_001166694.1:c.377+1351_377+1352dup	NP_001160166.1:n.377+1351_377+1352dup
NR_046313.1:n.878+1351_878+1352dup
XM_006720382.1:c.176+1351_176+1352dup	XP_006720445.1:n.176+1351_176+1352dup
XM_011521173.1:c.296+1351_296+1352dup	XP_011519475.1:n.296+1351_296+1352dup
XM_006720382.3:c.176+1351_176+1352dup	XP_006720445.1:n.176+1351_176+1352dup
NM_000743.5:c.377+1351_377+1352dup MANE Select	NP_000734.2:n.377+1351_377+1352dup
NM_001166694.2:c.377+1351_377+1352dup	NP_001160166.1:n.377+1351_377+1352dup
NR_046313.2:n.579+1351_579+1352dup