Canonical Allele Identifier: CA1308835911

Gene: CHRNA1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174757676C= , CM000664.2:g.174757676C=	GRCh38
NC_000002.11:g.175622404C= , CM000664.1:g.175622404C=	GRCh37
NC_000002.10:g.175330650C=	NCBI36
NG_008172.1:g.11797G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000079.4:c.235-1G= MANE Select	NP_000070.1:n.235-1G=
ENST00000348749.9:c.235-1G= MANE Select	ENSP00000261008.5:n.235-1G=
NM_000079.3:c.235-1G=	NP_000070.1:n.235-1G=
NM_001039523.2:c.310-1G=	NP_001034612.1:n.310-1G=
NM_001039523.3:c.310-1G=	NP_001034612.1:n.310-1G=
ENST00000261007.9:c.310-1G=	ENSP00000261007.5:n.310-1G=
ENST00000409219.5:c.235-1G=	ENSP00000386611.1:n.235-1G=
ENST00000409323.1:c.235-1G=	ENSP00000386684.1:n.235-1G=
ENST00000409542.5:c.234+1655G=	ENSP00000387026.1:n.234+1655G=
ENST00000435083.5:c.234+1655G=	ENSP00000395805.1:n.234+1655G=
ENST00000636168.2:c.-255-1G=	ENSP00000490338.2:n.-255-1G=
ENST00000672640.1:c.-255-1G=	ENSP00000500507.1:n.-255-1G=
XM_017003256.1:c.331-1G=	XP_016858745.1:n.331-1G=
XM_017003257.1:c.256-1G=	XP_016858746.1:n.256-1G=