Canonical Allele Identifier: CA2804872155

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595895_78595896insCTCC , CM000677.2:g.78595895_78595896insCTCC	GRCh38
NC_000015.9:g.78888237_78888238insCTCC , CM000677.1:g.78888237_78888238insCTCC	GRCh37
NC_000015.8:g.76675292_76675293insCTCC	NCBI36
NG_016143.1:g.30402_30403insAGGG
NG_023328.1:g.35376_35377insCTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.*710_*711insAGGG MANE Select	ENSP00000315602.5:n.*710_*711insAGGG
ENST00000326828.5:c.*710_*711insAGGG	ENSP00000315602.5:n.*710_*711insAGGG
ENST00000348639.7:c.1390-2703_1390-2702insAGGG	ENSP00000267951.4:n.1390-2703_1390-2702insAGGG
ENST00000559002.5:n.193+646_193+647insAGGG
ENST00000559658.5:c.*64+646_*64+647insAGGG	ENSP00000452896.1:n.*64+646_*64+647insAGGG
NM_000743.4:c.*710_*711insAGGG	NP_000734.2:n.*710_*711insAGGG
NM_001166694.1:c.1390-2703_1390-2702insAGGG	NP_001160166.1:n.1390-2703_1390-2702insAGGG
NR_046313.1:n.2083+646_2083+647insAGGG
XM_006720382.1:c.*710_*711insAGGG	XP_006720445.1:n.*710_*711insAGGG
XM_011521173.1:c.*710_*711insAGGG	XP_011519475.1:n.*710_*711insAGGG
XM_006720382.3:c.*710_*711insAGGG	XP_006720445.1:n.*710_*711insAGGG
NM_000743.5:c.*710_*711insAGGG MANE Select	NP_000734.2:n.*710_*711insAGGG
NM_001166694.2:c.1390-2703_1390-2702insAGGG	NP_001160166.1:n.1390-2703_1390-2702insAGGG
NR_046313.2:n.1784+646_1784+647insAGGG