Canonical Allele Identifier: CA409632137

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981018T>A (hg19) ; chr20:g.63349666T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349666T>A , CM000682.2:g.63349666T>A	GRCh38
NC_000020.10:g.61981018T>A , CM000682.1:g.61981018T>A	GRCh37
NC_000020.9:g.61451462T>A	NCBI36
NG_011931.1:g.16678A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370263.9:c.1745A>T MANE Select	ENSP00000359285.4:p.Asp582Val
ENST00000370263.8:c.1745A>T	ENSP00000359285.4:p.Asp582Val
ENST00000463705.5:n.2393A>T
ENST00000467563.3:n.1815A>T
ENST00000498043.6:c.1769A>T
ENST00000615287.4:c.1532A>T	ENSP00000483388.1:p.Asp511Val
ENST00000627000.1:c.*1434A>T	ENSP00000486914.1:n.*1434A>T
ENST00000630240.1:n.1466A>T
NM_000744.6:c.1745A>T	NP_000735.1:p.Asp582Val
NM_001256573.1:c.1217A>T	NP_001243502.1:p.Asp406Val
NR_046317.1:n.2001A>T
XM_011528524.1:c.1532A>T	XP_011526826.1:p.Asp511Val
XM_017027625.2:c.1217A>T	XP_016883114.1:p.Asp406Val
XM_024451822.1:c.1217A>T	XP_024307590.1:p.Asp406Val
NM_001256573.2:c.1217A>T	NP_001243502.1:p.Asp406Val
NR_046317.2:n.1954A>T
NM_000744.7:c.1745A>T MANE Select	NP_000735.1:p.Asp582Val