Canonical Allele Identifier: CA2629793601

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78596057-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78596059del , CM000677.2:g.78596059del	GRCh38
NC_000015.9:g.78888401del , CM000677.1:g.78888401del	GRCh37
NC_000015.8:g.76675456del	NCBI36
NG_016143.1:g.30238del
NG_023328.1:g.35540del

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.*546del MANE Select	ENSP00000315602.5:n.*546del
ENST00000326828.5:c.*546del	ENSP00000315602.5:n.*546del
ENST00000348639.7:c.1390-2867del	ENSP00000267951.4:n.1390-2867del
ENST00000559002.5:n.193+482del
ENST00000559658.5:c.*64+482del	ENSP00000452896.1:n.*64+482del
NM_000743.4:c.*546del	NP_000734.2:n.*546del
NM_001166694.1:c.1390-2867del	NP_001160166.1:n.1390-2867del
NR_046313.1:n.2083+482del
XM_006720382.1:c.*546del	XP_006720445.1:n.*546del
XM_011521173.1:c.*546del	XP_011519475.1:n.*546del
XM_006720382.3:c.*546del	XP_006720445.1:n.*546del
NM_000743.5:c.*546del MANE Select	NP_000734.2:n.*546del
NM_001166694.2:c.1390-2867del	NP_001160166.1:n.1390-2867del
NR_046313.2:n.1784+482del