Canonical Allele Identifier: CA2629789133

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78602125-AGTTTTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602128_78602133del , CM000677.2:g.78602128_78602133del	GRCh38
NC_000015.9:g.78894470_78894475del , CM000677.1:g.78894470_78894475del	GRCh37
NC_000015.8:g.76681525_76681530del	NCBI36
NG_016143.1:g.24165_24170del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.511_516del MANE Select	ENSP00000315602.5:p.Gln171_Asn172del
ENST00000326828.5:c.511_516del	ENSP00000315602.5:p.Gln171_Asn172del
ENST00000348639.7:c.511_516del	ENSP00000267951.4:p.Gln171_Asn172del
ENST00000558903.1:n.218_223del
ENST00000559658.5:c.511_516del	ENSP00000452896.1:p.Gln171_Asn172del
NM_000743.4:c.511_516del	NP_000734.2:p.Gln171_Asn172del
NM_001166694.1:c.511_516del	NP_001160166.1:p.Gln171_Asn172del
NR_046313.1:n.1012_1017del
XM_006720382.1:c.310_315del	XP_006720445.1:p.Gln104_Asn105del
XM_011521173.1:c.430_435del	XP_011519475.1:p.Gln144_Asn145del
XM_006720382.3:c.310_315del	XP_006720445.1:p.Gln104_Asn105del
NM_000743.5:c.511_516del MANE Select	NP_000734.2:p.Gln171_Asn172del
NM_001166694.2:c.511_516del	NP_001160166.1:p.Gln171_Asn172del
NR_046313.2:n.713_718del