Canonical Allele Identifier: CA393585631

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78602016-A-T
• MyVariant Identifiers: chr15:g.78894358A>T (hg19) ; chr15:g.78602016A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602016A>T , CM000677.2:g.78602016A>T	GRCh38
NC_000015.9:g.78894358A>T , CM000677.1:g.78894358A>T	GRCh37
NC_000015.8:g.76681413A>T	NCBI36
NG_016143.1:g.24280T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.626T>A MANE Select	ENSP00000315602.5:p.Ile209Asn
ENST00000326828.5:c.626T>A	ENSP00000315602.5:p.Ile209Asn
ENST00000348639.7:c.626T>A	ENSP00000267951.4:p.Ile209Asn
ENST00000558903.1:n.333T>A
ENST00000559658.5:c.626T>A	ENSP00000452896.1:p.Ile209Asn
NM_000743.4:c.626T>A	NP_000734.2:p.Ile209Asn
NM_001166694.1:c.626T>A	NP_001160166.1:p.Ile209Asn
NR_046313.1:n.1127T>A
XM_006720382.1:c.425T>A	XP_006720445.1:p.Ile142Asn
XM_011521173.1:c.545T>A	XP_011519475.1:p.Ile182Asn
XM_006720382.3:c.425T>A	XP_006720445.1:p.Ile142Asn
NM_000743.5:c.626T>A MANE Select	NP_000734.2:p.Ile209Asn
NM_001166694.2:c.626T>A	NP_001160166.1:p.Ile209Asn
NR_046313.2:n.828T>A