Canonical Allele Identifier: CA409638071

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61982222A>T (hg19) ; chr20:g.63350870A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350870A>T , CM000682.2:g.63350870A>T	GRCh38
NC_000020.10:g.61982222A>T , CM000682.1:g.61982222A>T	GRCh37
NC_000020.9:g.61452666A>T	NCBI36
NG_011931.1:g.15474T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.541T>A MANE Select	ENSP00000359285.4:p.Ser181Thr
ENST00000370263.8:c.541T>A	ENSP00000359285.4:p.Ser181Thr
ENST00000463705.5:n.1189T>A
ENST00000467563.3:n.611T>A
ENST00000498043.6:c.565T>A
ENST00000615287.4:c.328T>A	ENSP00000483388.1:p.Ser110Thr
ENST00000627000.1:c.*230T>A	ENSP00000486914.1:n.*230T>A
ENST00000630240.1:n.262T>A
NM_000744.6:c.541T>A	NP_000735.1:p.Ser181Thr
NM_001256573.1:c.13T>A	NP_001243502.1:p.Ser5Thr
NR_046317.1:n.797T>A
XM_011528524.1:c.328T>A	XP_011526826.1:p.Ser110Thr
XM_017027625.2:c.13T>A	XP_016883114.1:p.Ser5Thr
XM_024451822.1:c.13T>A	XP_024307590.1:p.Ser5Thr
NM_001256573.2:c.13T>A	NP_001243502.1:p.Ser5Thr
NR_046317.2:n.750T>A
NM_000744.7:c.541T>A MANE Select	NP_000735.1:p.Ser181Thr