Canonical Allele Identifier: CA2629793247

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78595892-A-ACCAC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595894_78595895insACCC , CM000677.2:g.78595894_78595895insACCC	GRCh38
NC_000015.9:g.78888236_78888237insACCC , CM000677.1:g.78888236_78888237insACCC	GRCh37
NC_000015.8:g.76675291_76675292insACCC	NCBI36
NG_016143.1:g.30403_30404insGTGG
NG_023328.1:g.35375_35376insACCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.*711_*712insGTGG MANE Select	ENSP00000315602.5:n.*711_*712insGTGG
ENST00000326828.5:c.*711_*712insGTGG	ENSP00000315602.5:n.*711_*712insGTGG
ENST00000348639.7:c.1390-2702_1390-2701insGTGG	ENSP00000267951.4:n.1390-2702_1390-2701insGTGG
ENST00000559002.5:n.193+647_193+648insGTGG
ENST00000559658.5:c.*64+647_*64+648insGTGG	ENSP00000452896.1:n.*64+647_*64+648insGTGG
NM_000743.4:c.*711_*712insGTGG	NP_000734.2:n.*711_*712insGTGG
NM_001166694.1:c.1390-2702_1390-2701insGTGG	NP_001160166.1:n.1390-2702_1390-2701insGTGG
NR_046313.1:n.2083+647_2083+648insGTGG
XM_006720382.1:c.*711_*712insGTGG	XP_006720445.1:n.*711_*712insGTGG
XM_011521173.1:c.*711_*712insGTGG	XP_011519475.1:n.*711_*712insGTGG
XM_006720382.3:c.*711_*712insGTGG	XP_006720445.1:n.*711_*712insGTGG
NM_000743.5:c.*711_*712insGTGG MANE Select	NP_000734.2:n.*711_*712insGTGG
NM_001166694.2:c.1390-2702_1390-2701insGTGG	NP_001160166.1:n.1390-2702_1390-2701insGTGG
NR_046313.2:n.1784+647_1784+648insGTGG