Canonical Allele Identifier: CA511339155

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61982148C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350796C>T , CM000682.2:g.63350796C>T	GRCh38
NC_000020.10:g.61982148C>T , CM000682.1:g.61982148C>T	GRCh37
NC_000020.9:g.61452592C>T	NCBI36
NG_011931.1:g.15548G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.615G>A MANE Select	ENSP00000359285.4:p.Glu205=
ENST00000370263.8:c.615G>A	ENSP00000359285.4:p.Glu205=
ENST00000463705.5:n.1263G>A
ENST00000467563.3:n.685G>A
ENST00000498043.6:c.639G>A
ENST00000615287.4:c.402G>A	ENSP00000483388.1:p.Glu134=
ENST00000627000.1:c.*304G>A	ENSP00000486914.1:n.*304G>A
ENST00000630240.1:n.336G>A
NM_000744.6:c.615G>A	NP_000735.1:p.Glu205=
NM_001256573.1:c.87G>A	NP_001243502.1:p.Glu29=
NR_046317.1:n.871G>A
XM_011528524.1:c.402G>A	XP_011526826.1:p.Glu134=
XM_017027625.2:c.87G>A	XP_016883114.1:p.Glu29=
XM_024451822.1:c.87G>A	XP_024307590.1:p.Glu29=
NM_001256573.2:c.87G>A	NP_001243502.1:p.Glu29=
NR_046317.2:n.824G>A
NM_000744.7:c.615G>A MANE Select	NP_000735.1:p.Glu205=