Canonical Allele Identifier: CA343921

Gene: CHRNA4

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350404C>T , CM000682.2:g.63350404C>T	GRCh38
NC_000020.10:g.61981756C>T , CM000682.1:g.61981756C>T	GRCh37
NC_000020.9:g.61452200C>T	NCBI36
NG_011931.1:g.15940G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1007G>A MANE Select	ENSP00000359285.4:p.Arg336His
ENST00000370263.8:c.1007G>A	ENSP00000359285.4:p.Arg336His
ENST00000463705.5:n.1655G>A
ENST00000467563.3:n.1077G>A
ENST00000498043.6:c.1031G>A
ENST00000615287.4:c.794G>A	ENSP00000483388.1:p.Arg265His
ENST00000627000.1:c.*696G>A	ENSP00000486914.1:n.*696G>A
ENST00000630240.1:n.728G>A
NM_000744.6:c.1007G>A	NP_000735.1:p.Arg336His
NM_001256573.1:c.479G>A	NP_001243502.1:p.Arg160His
NR_046317.1:n.1263G>A
XM_011528524.1:c.794G>A	XP_011526826.1:p.Arg265His
XM_017027625.2:c.479G>A	XP_016883114.1:p.Arg160His
XM_024451822.1:c.479G>A	XP_024307590.1:p.Arg160His
NM_001256573.2:c.479G>A	NP_001243502.1:p.Arg160His
NR_046317.2:n.1216G>A
NM_000744.7:c.1007G>A MANE Select	NP_000735.1:p.Arg336His