Canonical Allele Identifier: CA971782769

Gene: CHRNA3

Linked Data

• dbSNP Id: rs2053208051
• gnomAD v3: 15-78601920-G-GT
• gnomAD v4: 15-78601920-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601920_78601921insT , CM000677.2:g.78601920_78601921insT	GRCh38
NC_000015.9:g.78894262_78894263insT , CM000677.1:g.78894262_78894263insT	GRCh37
NC_000015.8:g.76681317_76681318insT	NCBI36
NG_016143.1:g.24375_24376insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.721_722insA MANE Select	ENSP00000315602.5:p.Pro241HisfsTer?
ENST00000326828.5:c.721_722insA	ENSP00000315602.5:p.Pro241HisfsTer?
ENST00000348639.7:c.721_722insA	ENSP00000267951.4:p.Pro241HisfsTer?
ENST00000558903.1:n.428_429insA
ENST00000559658.5:c.721_722insA	ENSP00000452896.1:p.Pro241HisfsTer?
NM_000743.4:c.721_722insA	NP_000734.2:p.Pro241HisfsTer?
NM_001166694.1:c.721_722insA	NP_001160166.1:p.Pro241HisfsTer?
NR_046313.1:n.1222_1223insA
XM_006720382.1:c.520_521insA	XP_006720445.1:p.Pro174HisfsTer?
XM_011521173.1:c.640_641insA	XP_011519475.1:p.Pro214HisfsTer?
XM_006720382.3:c.520_521insA	XP_006720445.1:p.Pro174HisfsTer?
NM_000743.5:c.721_722insA MANE Select	NP_000734.2:p.Pro241HisfsTer?
NM_001166694.2:c.721_722insA	NP_001160166.1:p.Pro241HisfsTer?
NR_046313.2:n.923_924insA