Canonical Allele Identifier: CA152387

Gene: CHRNA4

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350733A>G , CM000682.2:g.63350733A>G	GRCh38
NC_000020.10:g.61982085A>G , CM000682.1:g.61982085A>G	GRCh37
NC_000020.9:g.61452529A>G	NCBI36
NG_011931.1:g.15611T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.678T>C MANE Select	ENSP00000359285.4:p.Cys226=
ENST00000370263.8:c.678T>C	ENSP00000359285.4:p.Cys226=
ENST00000463705.5:n.1326T>C
ENST00000467563.3:n.748T>C
ENST00000498043.6:c.702T>C
ENST00000615287.4:c.465T>C	ENSP00000483388.1:p.Cys155=
ENST00000627000.1:c.*367T>C	ENSP00000486914.1:n.*367T>C
ENST00000630240.1:n.399T>C
NM_000744.6:c.678T>C	NP_000735.1:p.Cys226=
NM_001256573.1:c.150T>C	NP_001243502.1:p.Cys50=
NR_046317.1:n.934T>C
XM_011528524.1:c.465T>C	XP_011526826.1:p.Cys155=
XM_017027625.2:c.150T>C	XP_016883114.1:p.Cys50=
XM_024451822.1:c.150T>C	XP_024307590.1:p.Cys50=
NM_001256573.2:c.150T>C	NP_001243502.1:p.Cys50=
NR_046317.2:n.887T>C
NM_000744.7:c.678T>C MANE Select	NP_000735.1:p.Cys226=