Canonical Allele Identifier: CA2374748963

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63359538C= , CM000682.2:g.63359538C=	GRCh38
NC_000020.10:g.61990890C= , CM000682.1:g.61990890C=	GRCh37
NC_000020.9:g.61461334C=	NCBI36
NG_011931.1:g.6806G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000370263.9:c.228+10G= MANE Select	ENSP00000359285.4:n.228+10G=
ENST00000636481.1:n.36+10G=
ENST00000636726.1:n.33+10G=
ENST00000675470.1:c.228+10G=	ENSP00000502096.1:n.228+10G=
ENST00000370263.8:c.228+10G=	ENSP00000359285.4:n.228+10G=
ENST00000463705.5:n.1032-8511G=
ENST00000467563.3:n.280+10G=
ENST00000498043.6:c.152+10G=
ENST00000615287.4:c.-86+10G=	ENSP00000483388.1:n.-86+10G=
ENST00000626188.1:n.302G=
ENST00000627000.1:c.228+10G=	ENSP00000486914.1:n.228+10G=
ENST00000628665.1:n.253+10G=
NM_000744.6:c.228+10G=	NP_000735.1:n.228+10G=
NM_001256573.1:c.-319+10G=	NP_001243502.1:n.-319+10G=
NR_046317.1:n.459+10G=
XM_017027625.2:c.-319+10G=	XP_016883114.1:n.-319+10G=
NM_001256573.2:c.-319+10G=	NP_001243502.1:n.-319+10G=
NR_046317.2:n.412+10G=
NM_000744.7:c.228+10G= MANE Select	NP_000735.1:n.228+10G=