Canonical Allele Identifier: CA2629793301

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78595895-C-CCCCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595895_78595896insCCCCT , CM000677.2:g.78595895_78595896insCCCCT	GRCh38
NC_000015.9:g.78888237_78888238insCCCCT , CM000677.1:g.78888237_78888238insCCCCT	GRCh37
NC_000015.8:g.76675292_76675293insCCCCT	NCBI36
NG_016143.1:g.30400_30401insAGGGG
NG_023328.1:g.35376_35377insCCCCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.*708_*709insAGGGG MANE Select	ENSP00000315602.5:n.*708_*709insAGGGG
ENST00000326828.5:c.*708_*709insAGGGG	ENSP00000315602.5:n.*708_*709insAGGGG
ENST00000348639.7:c.1390-2705_1390-2704insAGGGG	ENSP00000267951.4:n.1390-2705_1390-2704insAGGGG
ENST00000559002.5:n.193+644_193+645insAGGGG
ENST00000559658.5:c.*64+644_*64+645insAGGGG	ENSP00000452896.1:n.*64+644_*64+645insAGGGG
NM_000743.4:c.*708_*709insAGGGG	NP_000734.2:n.*708_*709insAGGGG
NM_001166694.1:c.1390-2705_1390-2704insAGGGG	NP_001160166.1:n.1390-2705_1390-2704insAGGGG
NR_046313.1:n.2083+644_2083+645insAGGGG
XM_006720382.1:c.*708_*709insAGGGG	XP_006720445.1:n.*708_*709insAGGGG
XM_011521173.1:c.*708_*709insAGGGG	XP_011519475.1:n.*708_*709insAGGGG
XM_006720382.3:c.*708_*709insAGGGG	XP_006720445.1:n.*708_*709insAGGGG
NM_000743.5:c.*708_*709insAGGGG MANE Select	NP_000734.2:n.*708_*709insAGGGG
NM_001166694.2:c.1390-2705_1390-2704insAGGGG	NP_001160166.1:n.1390-2705_1390-2704insAGGGG
NR_046313.2:n.1784+644_1784+645insAGGGG