Canonical Allele Identifier: CA409635918

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981801A>T (hg19) ; chr20:g.63350449A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350449A>T , CM000682.2:g.63350449A>T	GRCh38
NC_000020.10:g.61981801A>T , CM000682.1:g.61981801A>T	GRCh37
NC_000020.9:g.61452245A>T	NCBI36
NG_011931.1:g.15895T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.962T>A MANE Select	ENSP00000359285.4:p.Ile321Asn
ENST00000370263.8:c.962T>A	ENSP00000359285.4:p.Ile321Asn
ENST00000463705.5:n.1610T>A
ENST00000467563.3:n.1032T>A
ENST00000498043.6:c.986T>A
ENST00000615287.4:c.749T>A	ENSP00000483388.1:p.Ile250Asn
ENST00000627000.1:c.*651T>A	ENSP00000486914.1:n.*651T>A
ENST00000630240.1:n.683T>A
NM_000744.6:c.962T>A	NP_000735.1:p.Ile321Asn
NM_001256573.1:c.434T>A	NP_001243502.1:p.Ile145Asn
NR_046317.1:n.1218T>A
XM_011528524.1:c.749T>A	XP_011526826.1:p.Ile250Asn
XM_017027625.2:c.434T>A	XP_016883114.1:p.Ile145Asn
XM_024451822.1:c.434T>A	XP_024307590.1:p.Ile145Asn
NM_001256573.2:c.434T>A	NP_001243502.1:p.Ile145Asn
NR_046317.2:n.1171T>A
NM_000744.7:c.962T>A MANE Select	NP_000735.1:p.Ile321Asn