Canonical Allele Identifier: CA2374743080

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350636A= , CM000682.2:g.63350636A=	GRCh38
NC_000020.10:g.61981988A= , CM000682.1:g.61981988A=	GRCh37
NC_000020.9:g.61452432A=	NCBI36
NG_011931.1:g.15708T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.775T= MANE Select	ENSP00000359285.4:p.Cys259=
ENST00000370263.8:c.775T=	ENSP00000359285.4:p.Cys259=
ENST00000463705.5:n.1423T=
ENST00000467563.3:n.845T=
ENST00000498043.6:c.799T=
ENST00000615287.4:c.562T=	ENSP00000483388.1:p.Cys188=
ENST00000627000.1:c.*464T=	ENSP00000486914.1:n.*464T=
ENST00000630240.1:n.496T=
NM_000744.6:c.775T=	NP_000735.1:p.Cys259=
NM_001256573.1:c.247T=	NP_001243502.1:p.Cys83=
NR_046317.1:n.1031T=
XM_011528524.1:c.562T=	XP_011526826.1:p.Cys188=
XM_017027625.2:c.247T=	XP_016883114.1:p.Cys83=
XM_024451822.1:c.247T=	XP_024307590.1:p.Cys83=
NM_001256573.2:c.247T=	NP_001243502.1:p.Cys83=
NR_046317.2:n.984T=
NM_000744.7:c.775T= MANE Select	NP_000735.1:p.Cys259=