Canonical Allele Identifier: CA2189599088

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595968_78595970delinsCTG , CM000677.2:g.78595968_78595970delinsCTG	GRCh38
NC_000015.9:g.78888310_78888312delinsCTG , CM000677.1:g.78888310_78888312delinsCTG	GRCh37
NC_000015.8:g.76675365_76675367delinsCTG	NCBI36
NG_016143.1:g.30326_30328delinsCAG
NG_023328.1:g.35449_35451delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.*634_*636delinsCAG MANE Select	ENSP00000315602.5:n.*634_*636delinsCAG
ENST00000326828.5:c.*634_*636delinsCAG	ENSP00000315602.5:n.*634_*636delinsCAG
ENST00000348639.7:c.1390-2779_1390-2777delinsCAG	ENSP00000267951.4:n.1390-2779_1390-2777de...
ENST00000559002.5:n.193+570_193+572delinsCAG
ENST00000559658.5:c.*64+570_*64+572delinsCAG	ENSP00000452896.1:n.*64+570_*64+572delins...
NM_000743.4:c.*634_*636delinsCAG	NP_000734.2:n.*634_*636delinsCAG
NM_001166694.1:c.1390-2779_1390-2777delinsCAG	NP_001160166.1:n.1390-2779_1390-2777delin...
NR_046313.1:n.2083+570_2083+572delinsCAG
XM_006720382.1:c.*634_*636delinsCAG	XP_006720445.1:n.*634_*636delinsCAG
XM_011521173.1:c.*634_*636delinsCAG	XP_011519475.1:n.*634_*636delinsCAG
XM_006720382.3:c.*634_*636delinsCAG	XP_006720445.1:n.*634_*636delinsCAG
NM_000743.5:c.*634_*636delinsCAG MANE Select	NP_000734.2:n.*634_*636delinsCAG
NM_001166694.2:c.1390-2779_1390-2777delinsCAG	NP_001160166.1:n.1390-2779_1390-2777delin...
NR_046313.2:n.1784+570_1784+572delinsCAG