Canonical Allele Identifier: CA2374743009

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350511T= , CM000682.2:g.63350511T=	GRCh38
NC_000020.10:g.61981863T= , CM000682.1:g.61981863T=	GRCh37
NC_000020.9:g.61452307T=	NCBI36
NG_011931.1:g.15833A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.900A= MANE Select	ENSP00000359285.4:p.Ser300=
ENST00000370263.8:c.900A=	ENSP00000359285.4:p.Ser300=
ENST00000463705.5:n.1548A=
ENST00000467563.3:n.970A=
ENST00000498043.6:c.924A=
ENST00000615287.4:c.687A=	ENSP00000483388.1:p.Ser229=
ENST00000627000.1:c.*589A=	ENSP00000486914.1:n.*589A=
ENST00000630240.1:n.621A=
NM_000744.6:c.900A=	NP_000735.1:p.Ser300=
NM_001256573.1:c.372A=	NP_001243502.1:p.Ser124=
NR_046317.1:n.1156A=
XM_011528524.1:c.687A=	XP_011526826.1:p.Ser229=
XM_017027625.2:c.372A=	XP_016883114.1:p.Ser124=
XM_024451822.1:c.372A=	XP_024307590.1:p.Ser124=
NM_001256573.2:c.372A=	NP_001243502.1:p.Ser124=
NR_046317.2:n.1109A=
NM_000744.7:c.900A= MANE Select	NP_000735.1:p.Ser300=