Canonical Allele Identifier: CA2629793252

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78595892-A-ACTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595893_78595894insTCCC , CM000677.2:g.78595893_78595894insTCCC	GRCh38
NC_000015.9:g.78888235_78888236insTCCC , CM000677.1:g.78888235_78888236insTCCC	GRCh37
NC_000015.8:g.76675290_76675291insTCCC	NCBI36
NG_016143.1:g.30403_30404insGGAG
NG_023328.1:g.35374_35375insTCCC

Transcript Alleles

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