Canonical Allele Identifier: CA317431701

Gene: CHRNA4

Linked Data

• dbSNP Id: rs1027482616
• gnomAD v3: 20-63349754-C-CG
• gnomAD v4: 20-63349754-C-CG
• MyVariant Identifiers: chr20:g.61981106_61981107insG (hg19) ; chr20:g.63349754_63349755insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349754_63349755insG , CM000682.2:g.63349754_63349755insG	GRCh38
NC_000020.10:g.61981106_61981107insG , CM000682.1:g.61981106_61981107insG	GRCh37
NC_000020.9:g.61451550_61451551insG	NCBI36
NG_011931.1:g.16589_16590insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000370263.9:c.1656_1657insC MANE Select	ENSP00000359285.4:p.Ala553ArgfsTer?
ENST00000370263.8:c.1656_1657insC	ENSP00000359285.4:p.Ala553ArgfsTer?
ENST00000463705.5:n.2304_2305insC
ENST00000467563.3:n.1726_1727insC
ENST00000498043.6:c.1680_1681insC
ENST00000615287.4:c.1443_1444insC	ENSP00000483388.1:p.Ala482ArgfsTer?
ENST00000627000.1:c.*1345_*1346insC	ENSP00000486914.1:n.*1345_*1346insC
ENST00000630240.1:n.1377_1378insC
NM_000744.6:c.1656_1657insC	NP_000735.1:p.Ala553ArgfsTer?
NM_001256573.1:c.1128_1129insC	NP_001243502.1:p.Ala377ArgfsTer?
NR_046317.1:n.1912_1913insC
XM_011528524.1:c.1443_1444insC	XP_011526826.1:p.Ala482ArgfsTer?
XM_017027625.2:c.1128_1129insC	XP_016883114.1:p.Ala377ArgfsTer?
XM_024451822.1:c.1128_1129insC	XP_024307590.1:p.Ala377ArgfsTer?
NM_001256573.2:c.1128_1129insC	NP_001243502.1:p.Ala377ArgfsTer?
NR_046317.2:n.1865_1866insC
NM_000744.7:c.1656_1657insC MANE Select	NP_000735.1:p.Ala553ArgfsTer?