Canonical Allele Identifier: CA715959700

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1402967048
• gnomAD v3: 15-78596055-CATGGT-C
• gnomAD v4: 15-78596055-CATGGT-C
• MyVariant Identifiers: chr15:g.78888398_78888402del (hg19) ; chr15:g.78596056_78596060del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78596058_78596062del , CM000677.2:g.78596058_78596062del	GRCh38
NC_000015.9:g.78888400_78888404del , CM000677.1:g.78888400_78888404del	GRCh37
NC_000015.8:g.76675455_76675459del	NCBI36
NG_016143.1:g.30236_30240del
NG_023328.1:g.35539_35543del

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.*544_*548del MANE Select	ENSP00000315602.5:n.*544_*548del
ENST00000326828.5:c.*544_*548del	ENSP00000315602.5:n.*544_*548del
ENST00000348639.7:c.1390-2869_1390-2865del	ENSP00000267951.4:n.1390-2869_1390-2865de...
ENST00000559002.5:n.193+480_193+484del
ENST00000559658.5:c.*64+480_*64+484del	ENSP00000452896.1:n.*64+480_*64+484del
NM_000743.4:c.*544_*548del	NP_000734.2:n.*544_*548del
NM_001166694.1:c.1390-2869_1390-2865del	NP_001160166.1:n.1390-2869_1390-2865del
NR_046313.1:n.2083+480_2083+484del
XM_006720382.1:c.*544_*548del	XP_006720445.1:n.*544_*548del
XM_011521173.1:c.*544_*548del	XP_011519475.1:n.*544_*548del
XM_006720382.3:c.*544_*548del	XP_006720445.1:n.*544_*548del
NM_000743.5:c.*544_*548del MANE Select	NP_000734.2:n.*544_*548del
NM_001166694.2:c.1390-2869_1390-2865del	NP_001160166.1:n.1390-2869_1390-2865del
NR_046313.2:n.1784+480_1784+484del