Canonical Allele Identifier: CA2374743216

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350895C= , CM000682.2:g.63350895C=	GRCh38
NC_000020.10:g.61982247C= , CM000682.1:g.61982247C=	GRCh37
NC_000020.9:g.61452691C=	NCBI36
NG_011931.1:g.15449G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.516G= MANE Select	ENSP00000359285.4:p.Gln172=
ENST00000370263.8:c.516G=	ENSP00000359285.4:p.Gln172=
ENST00000463705.5:n.1164G=
ENST00000467563.3:n.586G=
ENST00000498043.6:c.540G=
ENST00000615287.4:c.303G=	ENSP00000483388.1:p.Gln101=
ENST00000627000.1:c.*205G=	ENSP00000486914.1:n.*205G=
ENST00000630240.1:n.237G=
NM_000744.6:c.516G=	NP_000735.1:p.Gln172=
NM_001256573.1:c.-13G=	NP_001243502.1:n.-13G=
NR_046317.1:n.772G=
XM_011528524.1:c.303G=	XP_011526826.1:p.Gln101=
XM_017027625.2:c.-13G=	XP_016883114.1:n.-13G=
XM_024451822.1:c.-13G=	XP_024307590.1:n.-13G=
NM_001256573.2:c.-13G=	NP_001243502.1:n.-13G=
NR_046317.2:n.725G=
NM_000744.7:c.516G= MANE Select	NP_000735.1:p.Gln172=