Canonical Allele Identifier: CA2189599090

Gene: CHRNA3

Linked Data

• dbSNP Id: rs2053101076
• gnomAD v4: 15-78595968-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595969_78595970del , CM000677.2:g.78595969_78595970del	GRCh38
NC_000015.9:g.78888311_78888312del , CM000677.1:g.78888311_78888312del	GRCh37
NC_000015.8:g.76675366_76675367del	NCBI36
NG_016143.1:g.30326_30327del
NG_023328.1:g.35450_35451del

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.*634_*635del MANE Select	ENSP00000315602.5:n.*634_*635del
ENST00000326828.5:c.*634_*635del	ENSP00000315602.5:n.*634_*635del
ENST00000348639.7:c.1390-2779_1390-2778del	ENSP00000267951.4:n.1390-2779_1390-2778de...
ENST00000559002.5:n.193+570_193+571del
ENST00000559658.5:c.*64+570_*64+571del	ENSP00000452896.1:n.*64+570_*64+571del
NM_000743.4:c.*634_*635del	NP_000734.2:n.*634_*635del
NM_001166694.1:c.1390-2779_1390-2778del	NP_001160166.1:n.1390-2779_1390-2778del
NR_046313.1:n.2083+570_2083+571del
XM_006720382.1:c.*634_*635del	XP_006720445.1:n.*634_*635del
XM_011521173.1:c.*634_*635del	XP_011519475.1:n.*634_*635del
XM_006720382.3:c.*634_*635del	XP_006720445.1:n.*634_*635del
NM_000743.5:c.*634_*635del MANE Select	NP_000734.2:n.*634_*635del
NM_001166694.2:c.1390-2779_1390-2778del	NP_001160166.1:n.1390-2779_1390-2778del
NR_046313.2:n.1784+570_1784+571del