Canonical Allele Identifier: CA2629793255

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78595892-A-ATCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595892_78595893insTCCC , CM000677.2:g.78595892_78595893insTCCC	GRCh38
NC_000015.9:g.78888234_78888235insTCCC , CM000677.1:g.78888234_78888235insTCCC	GRCh37
NC_000015.8:g.76675289_76675290insTCCC	NCBI36
NG_016143.1:g.30403_30404insGGGA
NG_023328.1:g.35373_35374insTCCC

Transcript Alleles

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