Canonical Allele Identifier: CA2189581263

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78596111_78596112delinsCA , CM000677.2:g.78596111_78596112delinsCA	GRCh38
NC_000015.9:g.78888453_78888454delinsCA , CM000677.1:g.78888453_78888454delinsCA	GRCh37
NC_000015.8:g.76675508_76675509delinsCA	NCBI36
NG_016143.1:g.30184_30185delinsTG
NG_023328.1:g.35592_35593delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.*492_*493delinsTG MANE Select	ENSP00000315602.5:n.*492_*493delinsTG
ENST00000326828.5:c.*492_*493delinsTG	ENSP00000315602.5:n.*492_*493delinsTG
ENST00000348639.7:c.1390-2921_1390-2920delinsTG	ENSP00000267951.4:n.1390-2921_1390-2920delinsTG
ENST00000559002.5:n.193+428_193+429delinsTG
ENST00000559658.5:c.*64+428_*64+429delinsTG	ENSP00000452896.1:n.*64+428_*64+429delinsTG
NM_000743.4:c.*492_*493delinsTG	NP_000734.2:n.*492_*493delinsTG
NM_001166694.1:c.1390-2921_1390-2920delinsTG	NP_001160166.1:n.1390-2921_1390-2920delinsTG
NR_046313.1:n.2083+428_2083+429delinsTG
XM_006720382.1:c.*492_*493delinsTG	XP_006720445.1:n.*492_*493delinsTG
XM_011521173.1:c.*492_*493delinsTG	XP_011519475.1:n.*492_*493delinsTG
XM_006720382.3:c.*492_*493delinsTG	XP_006720445.1:n.*492_*493delinsTG
NM_000743.5:c.*492_*493delinsTG MANE Select	NP_000734.2:n.*492_*493delinsTG
NM_001166694.2:c.1390-2921_1390-2920delinsTG	NP_001160166.1:n.1390-2921_1390-2920delinsTG
NR_046313.2:n.1784+428_1784+429delinsTG