Canonical Allele Identifier: CA1308832574

Gene: CHRNA1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174750122A= , CM000664.2:g.174750122A=	GRCh38
NC_000002.11:g.175614850A= , CM000664.1:g.175614850A=	GRCh37
NC_000002.10:g.175323096A=	NCBI36
NG_008172.1:g.19351T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000079.4:c.826T= MANE Select	NP_000070.1:p.Phe276=
ENST00000348749.9:c.826T= MANE Select	ENSP00000261008.5:p.Phe276=
NM_000079.3:c.826T=	NP_000070.1:p.Phe276=
NM_001039523.2:c.901T=	NP_001034612.1:p.Phe301=
NM_001039523.3:c.901T=	NP_001034612.1:p.Phe301=
ENST00000261007.9:c.901T=	ENSP00000261007.5:p.Phe301=
ENST00000409219.5:c.826T=	ENSP00000386611.1:p.Phe276=
ENST00000409542.5:c.580T=	ENSP00000387026.1:p.Phe194=
ENST00000435083.5:c.*470T=	ENSP00000395805.1:n.*470T=
ENST00000636168.2:c.337T=	ENSP00000490338.2:p.Phe113=
ENST00000672640.1:c.337T=	ENSP00000500507.1:p.Phe113=
XM_017003256.1:c.922T=	XP_016858745.1:p.Phe308=
XM_017003257.1:c.847T=	XP_016858746.1:p.Phe283=