Canonical Allele Identifier: CA619234985

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1350187773
• gnomAD v2: 15-78888236-C-CCCCG
• gnomAD v3: 15-78595894-C-CCCCG
• gnomAD v4: 15-78595894-C-CCCCG
• MyVariant Identifiers: chr15:g.78888236_78888237insCCCG (hg19) ; chr15:g.78595894_78595895insCCCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595895_78595896insCCGC , CM000677.2:g.78595895_78595896insCCGC	GRCh38
NC_000015.9:g.78888237_78888238insCCGC , CM000677.1:g.78888237_78888238insCCGC	GRCh37
NC_000015.8:g.76675292_76675293insCCGC	NCBI36
NG_016143.1:g.30401_30402insCGGG
NG_023328.1:g.35376_35377insCCGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.*709_*710insCGGG MANE Select	ENSP00000315602.5:n.*709_*710insCGGG
ENST00000326828.5:c.*709_*710insCGGG	ENSP00000315602.5:n.*709_*710insCGGG
ENST00000348639.7:c.1390-2704_1390-2703insCGGG	ENSP00000267951.4:n.1390-2704_1390-2703insCGGG
ENST00000559002.5:n.193+645_193+646insCGGG
ENST00000559658.5:c.*64+645_*64+646insCGGG	ENSP00000452896.1:n.*64+645_*64+646insCGGG
NM_000743.4:c.*709_*710insCGGG	NP_000734.2:n.*709_*710insCGGG
NM_001166694.1:c.1390-2704_1390-2703insCGGG	NP_001160166.1:n.1390-2704_1390-2703insCGGG
NR_046313.1:n.2083+645_2083+646insCGGG
XM_006720382.1:c.*709_*710insCGGG	XP_006720445.1:n.*709_*710insCGGG
XM_011521173.1:c.*709_*710insCGGG	XP_011519475.1:n.*709_*710insCGGG
XM_006720382.3:c.*709_*710insCGGG	XP_006720445.1:n.*709_*710insCGGG
NM_000743.5:c.*709_*710insCGGG MANE Select	NP_000734.2:n.*709_*710insCGGG
NM_001166694.2:c.1390-2704_1390-2703insCGGG	NP_001160166.1:n.1390-2704_1390-2703insCGGG
NR_046313.2:n.1784+645_1784+646insCGGG