Canonical Allele Identifier: CA746455538

Gene: CHRNA4

Linked Data

• dbSNP Id: rs1257952896
• MyVariant Identifiers: chr20:g.61981777del (hg19) ; chr20:g.63350425del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350426del , CM000682.2:g.63350426del	GRCh38
NC_000020.10:g.61981778del , CM000682.1:g.61981778del	GRCh37
NC_000020.9:g.61452222del	NCBI36
NG_011931.1:g.15919del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.986del MANE Select	ENSP00000359285.4:p.Asn329ThrfsTer30
ENST00000370263.8:c.986del	ENSP00000359285.4:p.Asn329ThrfsTer30
ENST00000463705.5:n.1634del
ENST00000467563.3:n.1056del
ENST00000498043.6:c.1010del
ENST00000615287.4:c.773del	ENSP00000483388.1:p.Asn258ThrfsTer30
ENST00000627000.1:c.*675del	ENSP00000486914.1:n.*675del
ENST00000630240.1:n.707del
NM_000744.6:c.986del	NP_000735.1:p.Asn329ThrfsTer30
NM_001256573.1:c.458del	NP_001243502.1:p.Asn153ThrfsTer30
NR_046317.1:n.1242del
XM_011528524.1:c.773del	XP_011526826.1:p.Asn258ThrfsTer30
XM_017027625.2:c.458del	XP_016883114.1:p.Asn153ThrfsTer30
XM_024451822.1:c.458del	XP_024307590.1:p.Asn153ThrfsTer30
NM_001256573.2:c.458del	NP_001243502.1:p.Asn153ThrfsTer30
NR_046317.2:n.1195del
NM_000744.7:c.986del MANE Select	NP_000735.1:p.Asn329ThrfsTer30