Canonical Allele Identifier: CA1308834334

Gene: CHRNA1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174754246G= , CM000664.2:g.174754246G=	GRCh38
NC_000002.11:g.175618974G= , CM000664.1:g.175618974G=	GRCh37
NC_000002.10:g.175327220G=	NCBI36
NG_008172.1:g.15227C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636168.2:c.24C=	ENSP00000490338.2:p.Tyr8=
ENST00000672640.1:c.24C=	ENSP00000500507.1:p.Tyr8=
ENST00000261007.9:c.588C=	ENSP00000261007.5:p.Tyr196=
ENST00000348749.9:c.513C= MANE Select	ENSP00000261008.5:p.Tyr171=
ENST00000409219.5:c.513C=	ENSP00000386611.1:p.Tyr171=
ENST00000409323.1:c.513C=	ENSP00000386684.1:p.Tyr171=
ENST00000409542.5:c.267C=	ENSP00000387026.1:p.Tyr89=
ENST00000435083.5:c.*157C=	ENSP00000395805.1:n.*157C=
NM_000079.3:c.513C=	NP_000070.1:p.Tyr171=
NM_001039523.2:c.588C=	NP_001034612.1:p.Tyr196=
XM_017003256.1:c.609C=	XP_016858745.1:p.Tyr203=
XM_017003257.1:c.534C=	XP_016858746.1:p.Tyr178=
NM_000079.4:c.513C= MANE Select	NP_000070.1:p.Tyr171=
NM_001039523.3:c.588C=	NP_001034612.1:p.Tyr196=