Canonical Allele Identifier: CA1308832522

Gene: CHRNA1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174750002T= , CM000664.2:g.174750002T=	GRCh38
NC_000002.11:g.175614730T= , CM000664.1:g.175614730T=	GRCh37
NC_000002.10:g.175322976T=	NCBI36
NG_008172.1:g.19471A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636168.2:c.457A=	ENSP00000490338.2:p.Ile153=
ENST00000672640.1:c.457A=	ENSP00000500507.1:p.Ile153=
ENST00000261007.9:c.1021A=	ENSP00000261007.5:p.Ile341=
ENST00000348749.9:c.946A= MANE Select	ENSP00000261008.5:p.Ile316=
ENST00000409219.5:c.946A=	ENSP00000386611.1:p.Ile316=
ENST00000409542.5:c.700A=	ENSP00000387026.1:p.Ile234=
ENST00000435083.5:c.*590A=	ENSP00000395805.1:n.*590A=
NM_000079.3:c.946A=	NP_000070.1:p.Ile316=
NM_001039523.2:c.1021A=	NP_001034612.1:p.Ile341=
XM_017003256.1:c.1042A=	XP_016858745.1:p.Ile348=
XM_017003257.1:c.967A=	XP_016858746.1:p.Ile323=
NM_000079.4:c.946A= MANE Select	NP_000070.1:p.Ile316=
NM_001039523.3:c.1021A=	NP_001034612.1:p.Ile341=