Canonical Allele Identifier: CA1308832559

Gene: CHRNA1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174750076A= , CM000664.2:g.174750076A=	GRCh38
NC_000002.11:g.175614804A= , CM000664.1:g.175614804A=	GRCh37
NC_000002.10:g.175323050A=	NCBI36
NG_008172.1:g.19397T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636168.2:c.383T=	ENSP00000490338.2:p.Val128=
ENST00000672640.1:c.383T=	ENSP00000500507.1:p.Val128=
ENST00000261007.9:c.947T=	ENSP00000261007.5:p.Val316=
ENST00000348749.9:c.872T= MANE Select	ENSP00000261008.5:p.Val291=
ENST00000409219.5:c.872T=	ENSP00000386611.1:p.Val291=
ENST00000409542.5:c.626T=	ENSP00000387026.1:p.Val209=
ENST00000435083.5:c.*516T=	ENSP00000395805.1:n.*516T=
NM_000079.3:c.872T=	NP_000070.1:p.Val291=
NM_001039523.2:c.947T=	NP_001034612.1:p.Val316=
XM_017003256.1:c.968T=	XP_016858745.1:p.Val323=
XM_017003257.1:c.893T=	XP_016858746.1:p.Val298=
NM_000079.4:c.872T= MANE Select	NP_000070.1:p.Val291=
NM_001039523.3:c.947T=	NP_001034612.1:p.Val316=