Canonical Allele Identifier: CA511338524

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981236G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349884G>C , CM000682.2:g.63349884G>C	GRCh38
NC_000020.10:g.61981236G>C , CM000682.1:g.61981236G>C	GRCh37
NC_000020.9:g.61451680G>C	NCBI36
NG_011931.1:g.16460C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1527C>G MANE Select	ENSP00000359285.4:p.Ala509=
ENST00000370263.8:c.1527C>G	ENSP00000359285.4:p.Ala509=
ENST00000463705.5:n.2175C>G
ENST00000467563.3:n.1597C>G
ENST00000498043.6:c.1551C>G
ENST00000615287.4:c.1314C>G	ENSP00000483388.1:p.Ala438=
ENST00000627000.1:c.*1216C>G	ENSP00000486914.1:n.*1216C>G
ENST00000630240.1:n.1248C>G
NM_000744.6:c.1527C>G	NP_000735.1:p.Ala509=
NM_001256573.1:c.999C>G	NP_001243502.1:p.Ala333=
NR_046317.1:n.1783C>G
XM_011528524.1:c.1314C>G	XP_011526826.1:p.Ala438=
XM_017027625.2:c.999C>G	XP_016883114.1:p.Ala333=
XM_024451822.1:c.999C>G	XP_024307590.1:p.Ala333=
NM_001256573.2:c.999C>G	NP_001243502.1:p.Ala333=
NR_046317.2:n.1736C>G
NM_000744.7:c.1527C>G MANE Select	NP_000735.1:p.Ala509=