Canonical Allele Identifier: CA1308834330
Gene: CHRNA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.174754240G= , CM000664.2:g.174754240G= GRCh38
NC_000002.11:g.175618968G= , CM000664.1:g.175618968G= GRCh37
NC_000002.10:g.175327214G= NCBI36
NG_008172.1:g.15233C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000636168.2:c.30C= ENSP00000490338.2:p.Gly10=
ENST00000672640.1:c.30C= ENSP00000500507.1:p.Gly10=
ENST00000261007.9:c.594C= ENSP00000261007.5:p.Gly198=
ENST00000348749.9:c.519C= MANE Select ENSP00000261008.5:p.Gly173=
ENST00000409219.5:c.519C= ENSP00000386611.1:p.Gly173=
ENST00000409323.1:c.519C= ENSP00000386684.1:p.Gly173=
ENST00000409542.5:c.273C= ENSP00000387026.1:p.Gly91=
ENST00000435083.5:c.*163C= ENSP00000395805.1:n.*163C=
NM_000079.3:c.519C= NP_000070.1:p.Gly173=
NM_001039523.2:c.594C= NP_001034612.1:p.Gly198=
XM_017003256.1:c.615C= XP_016858745.1:p.Gly205=
XM_017003257.1:c.540C= XP_016858746.1:p.Gly180=
NM_000079.4:c.519C= MANE Select NP_000070.1:p.Gly173=
NM_001039523.3:c.594C= NP_001034612.1:p.Gly198=