Canonical Allele Identifier: CA409637463

Gene: CHRNA4

Linked Data

• COSMIC: COSM6160775
• MyVariant Identifiers: chr20:g.61982135C>A (hg19) ; chr20:g.63350783C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350783C>A , CM000682.2:g.63350783C>A	GRCh38
NC_000020.10:g.61982135C>A , CM000682.1:g.61982135C>A	GRCh37
NC_000020.9:g.61452579C>A	NCBI36
NG_011931.1:g.15561G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.628G>T MANE Select	ENSP00000359285.4:p.Val210Phe
ENST00000370263.8:c.628G>T	ENSP00000359285.4:p.Val210Phe
ENST00000463705.5:n.1276G>T
ENST00000467563.3:n.698G>T
ENST00000498043.6:c.652G>T
ENST00000615287.4:c.415G>T	ENSP00000483388.1:p.Val139Phe
ENST00000627000.1:c.*317G>T	ENSP00000486914.1:n.*317G>T
ENST00000630240.1:n.349G>T
NM_000744.6:c.628G>T	NP_000735.1:p.Val210Phe
NM_001256573.1:c.100G>T	NP_001243502.1:p.Val34Phe
NR_046317.1:n.884G>T
XM_011528524.1:c.415G>T	XP_011526826.1:p.Val139Phe
XM_017027625.2:c.100G>T	XP_016883114.1:p.Val34Phe
XM_024451822.1:c.100G>T	XP_024307590.1:p.Val34Phe
NM_001256573.2:c.100G>T	NP_001243502.1:p.Val34Phe
NR_046317.2:n.837G>T
NM_000744.7:c.628G>T MANE Select	NP_000735.1:p.Val210Phe