Canonical Allele Identifier: CA409636599

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981942T>A (hg19) ; chr20:g.63350590T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350590T>A , CM000682.2:g.63350590T>A	GRCh38
NC_000020.10:g.61981942T>A , CM000682.1:g.61981942T>A	GRCh37
NC_000020.9:g.61452386T>A	NCBI36
NG_011931.1:g.15754A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.821A>T MANE Select	ENSP00000359285.4:p.Lys274Met
ENST00000370263.8:c.821A>T	ENSP00000359285.4:p.Lys274Met
ENST00000463705.5:n.1469A>T
ENST00000467563.3:n.891A>T
ENST00000498043.6:c.845A>T
ENST00000615287.4:c.608A>T	ENSP00000483388.1:p.Lys203Met
ENST00000627000.1:c.*510A>T	ENSP00000486914.1:n.*510A>T
ENST00000630240.1:n.542A>T
NM_000744.6:c.821A>T	NP_000735.1:p.Lys274Met
NM_001256573.1:c.293A>T	NP_001243502.1:p.Lys98Met
NR_046317.1:n.1077A>T
XM_011528524.1:c.608A>T	XP_011526826.1:p.Lys203Met
XM_017027625.2:c.293A>T	XP_016883114.1:p.Lys98Met
XM_024451822.1:c.293A>T	XP_024307590.1:p.Lys98Met
NM_001256573.2:c.293A>T	NP_001243502.1:p.Lys98Met
NR_046317.2:n.1030A>T
NM_000744.7:c.821A>T MANE Select	NP_000735.1:p.Lys274Met