Canonical Allele Identifier: CA2596563645

Gene: CHRNA3

Linked Data

• gnomAD v3: 15-78617135-T-TCGGGGAAGGAAG
• gnomAD v4: 15-78617135-T-TCGGGGAAGGAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78617137_78617148dup , CM000677.2:g.78617137_78617148dup	GRCh38
NC_000015.9:g.78909479_78909490dup , CM000677.1:g.78909479_78909490dup	GRCh37
NC_000015.8:g.76696534_76696545dup	NCBI36
NG_016143.1:g.9149_9160dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.268-14_268-3dup MANE Select	ENSP00000315602.5:n.268-14_268-3dup
ENST00000326828.5:c.268-14_268-3dup	ENSP00000315602.5:n.268-14_268-3dup
ENST00000348639.7:c.268-14_268-3dup	ENSP00000267951.4:n.268-14_268-3dup
ENST00000559658.5:c.268-14_268-3dup	ENSP00000452896.1:n.268-14_268-3dup
NM_000743.4:c.268-14_268-3dup	NP_000734.2:n.268-14_268-3dup
NM_001166694.1:c.268-14_268-3dup	NP_001160166.1:n.268-14_268-3dup
NR_046313.1:n.769-14_769-3dup
XM_006720382.1:c.67-14_67-3dup	XP_006720445.1:n.67-14_67-3dup
XM_011521173.1:c.187-14_187-3dup	XP_011519475.1:n.187-14_187-3dup
XM_006720382.3:c.67-14_67-3dup	XP_006720445.1:n.67-14_67-3dup
NM_000743.5:c.268-14_268-3dup MANE Select	NP_000734.2:n.268-14_268-3dup
NM_001166694.2:c.268-14_268-3dup	NP_001160166.1:n.268-14_268-3dup
NR_046313.2:n.470-14_470-3dup