Canonical Allele Identifier: CA409637299

Gene: CHRNA4

Linked Data

• gnomAD v3: 20-63350756-T-C
• gnomAD v4: 20-63350756-T-C
• MyVariant Identifiers: chr20:g.61982108T>C (hg19) ; chr20:g.63350756T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350756T>C , CM000682.2:g.63350756T>C	GRCh38
NC_000020.10:g.61982108T>C , CM000682.1:g.61982108T>C	GRCh37
NC_000020.9:g.61452552T>C	NCBI36
NG_011931.1:g.15588A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.655A>G MANE Select	ENSP00000359285.4:p.Asn219Asp
ENST00000370263.8:c.655A>G	ENSP00000359285.4:p.Asn219Asp
ENST00000463705.5:n.1303A>G
ENST00000467563.3:n.725A>G
ENST00000498043.6:c.679A>G
ENST00000615287.4:c.442A>G	ENSP00000483388.1:p.Asn148Asp
ENST00000627000.1:c.*344A>G	ENSP00000486914.1:n.*344A>G
ENST00000630240.1:n.376A>G
NM_000744.6:c.655A>G	NP_000735.1:p.Asn219Asp
NM_001256573.1:c.127A>G	NP_001243502.1:p.Asn43Asp
NR_046317.1:n.911A>G
XM_011528524.1:c.442A>G	XP_011526826.1:p.Asn148Asp
XM_017027625.2:c.127A>G	XP_016883114.1:p.Asn43Asp
XM_024451822.1:c.127A>G	XP_024307590.1:p.Asn43Asp
NM_001256573.2:c.127A>G	NP_001243502.1:p.Asn43Asp
NR_046317.2:n.864A>G
NM_000744.7:c.655A>G MANE Select	NP_000735.1:p.Asn219Asp