Canonical Allele Identifier: CA511338968

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981983G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350631G>C , CM000682.2:g.63350631G>C	GRCh38
NC_000020.10:g.61981983G>C , CM000682.1:g.61981983G>C	GRCh37
NC_000020.9:g.61452427G>C	NCBI36
NG_011931.1:g.15713C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.780C>G MANE Select	ENSP00000359285.4:p.Leu260=
ENST00000370263.8:c.780C>G	ENSP00000359285.4:p.Leu260=
ENST00000463705.5:n.1428C>G
ENST00000467563.3:n.850C>G
ENST00000498043.6:c.804C>G
ENST00000615287.4:c.567C>G	ENSP00000483388.1:p.Leu189=
ENST00000627000.1:c.*469C>G	ENSP00000486914.1:n.*469C>G
ENST00000630240.1:n.501C>G
NM_000744.6:c.780C>G	NP_000735.1:p.Leu260=
NM_001256573.1:c.252C>G	NP_001243502.1:p.Leu84=
NR_046317.1:n.1036C>G
XM_011528524.1:c.567C>G	XP_011526826.1:p.Leu189=
XM_017027625.2:c.252C>G	XP_016883114.1:p.Leu84=
XM_024451822.1:c.252C>G	XP_024307590.1:p.Leu84=
NM_001256573.2:c.252C>G	NP_001243502.1:p.Leu84=
NR_046317.2:n.989C>G
NM_000744.7:c.780C>G MANE Select	NP_000735.1:p.Leu260=