Canonical Allele Identifier: CA2629788894

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78601820-G-GGTC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601821_78601823dup , CM000677.2:g.78601821_78601823dup	GRCh38
NC_000015.9:g.78894163_78894165dup , CM000677.1:g.78894163_78894165dup	GRCh37
NC_000015.8:g.76681218_76681220dup	NCBI36
NG_016143.1:g.24473_24475dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.819_821dup MANE Select	ENSP00000315602.5:p.Thr274_Leu275insThr
ENST00000326828.5:c.819_821dup	ENSP00000315602.5:p.Thr274_Leu275insThr
ENST00000348639.7:c.819_821dup	ENSP00000267951.4:p.Thr274_Leu275insThr
ENST00000558903.1:n.526_528dup
ENST00000559658.5:c.819_821dup	ENSP00000452896.1:p.Thr274_Leu275insThr
NM_000743.4:c.819_821dup	NP_000734.2:p.Thr274_Leu275insThr
NM_001166694.1:c.819_821dup	NP_001160166.1:p.Thr274_Leu275insThr
NR_046313.1:n.1320_1322dup
XM_006720382.1:c.618_620dup	XP_006720445.1:p.Thr207_Leu208insThr
XM_011521173.1:c.738_740dup	XP_011519475.1:p.Thr247_Leu248insThr
XM_006720382.3:c.618_620dup	XP_006720445.1:p.Thr207_Leu208insThr
NM_000743.5:c.819_821dup MANE Select	NP_000734.2:p.Thr274_Leu275insThr
NM_001166694.2:c.819_821dup	NP_001160166.1:p.Thr274_Leu275insThr
NR_046313.2:n.1021_1023dup