Canonical Allele Identifier: CA511338791

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981788G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350436G>T , CM000682.2:g.63350436G>T	GRCh38
NC_000020.10:g.61981788G>T , CM000682.1:g.61981788G>T	GRCh37
NC_000020.9:g.61452232G>T	NCBI36
NG_011931.1:g.15908C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370263.9:c.975C>A MANE Select	ENSP00000359285.4:p.Val325=
ENST00000370263.8:c.975C>A	ENSP00000359285.4:p.Val325=
ENST00000463705.5:n.1623C>A
ENST00000467563.3:n.1045C>A
ENST00000498043.6:c.999C>A
ENST00000615287.4:c.762C>A	ENSP00000483388.1:p.Val254=
ENST00000627000.1:c.*664C>A	ENSP00000486914.1:n.*664C>A
ENST00000630240.1:n.696C>A
NM_000744.6:c.975C>A	NP_000735.1:p.Val325=
NM_001256573.1:c.447C>A	NP_001243502.1:p.Val149=
NR_046317.1:n.1231C>A
XM_011528524.1:c.762C>A	XP_011526826.1:p.Val254=
XM_017027625.2:c.447C>A	XP_016883114.1:p.Val149=
XM_024451822.1:c.447C>A	XP_024307590.1:p.Val149=
NM_001256573.2:c.447C>A	NP_001243502.1:p.Val149=
NR_046317.2:n.1184C>A
NM_000744.7:c.975C>A MANE Select	NP_000735.1:p.Val325=