Canonical Allele Identifier: CA1308834327

Gene: CHRNA1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174754233C= , CM000664.2:g.174754233C=	GRCh38
NC_000002.11:g.175618961C= , CM000664.1:g.175618961C=	GRCh37
NC_000002.10:g.175327207C=	NCBI36
NG_008172.1:g.15240G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636168.2:c.37G=	ENSP00000490338.2:p.Val13=
ENST00000672640.1:c.37G=	ENSP00000500507.1:p.Val13=
ENST00000261007.9:c.601G=	ENSP00000261007.5:p.Val201=
ENST00000348749.9:c.526G= MANE Select	ENSP00000261008.5:p.Val176=
ENST00000409219.5:c.526G=	ENSP00000386611.1:p.Val176=
ENST00000409323.1:c.526G=	ENSP00000386684.1:p.Val176=
ENST00000409542.5:c.280G=	ENSP00000387026.1:p.Val94=
ENST00000435083.5:c.*170G=	ENSP00000395805.1:n.*170G=
NM_000079.3:c.526G=	NP_000070.1:p.Val176=
NM_001039523.2:c.601G=	NP_001034612.1:p.Val201=
XM_017003256.1:c.622G=	XP_016858745.1:p.Val208=
XM_017003257.1:c.547G=	XP_016858746.1:p.Val183=
NM_000079.4:c.526G= MANE Select	NP_000070.1:p.Val176=
NM_001039523.3:c.601G=	NP_001034612.1:p.Val201=