Canonical Allele Identifier: CA1308834329
Gene: CHRNA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.174754239A= , CM000664.2:g.174754239A= GRCh38
NC_000002.11:g.175618967A= , CM000664.1:g.175618967A= GRCh37
NC_000002.10:g.175327213A= NCBI36
NG_008172.1:g.15234T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000636168.2:c.31T= ENSP00000490338.2:p.Ser11=
ENST00000672640.1:c.31T= ENSP00000500507.1:p.Ser11=
ENST00000261007.9:c.595T= ENSP00000261007.5:p.Ser199=
ENST00000348749.9:c.520T= MANE Select ENSP00000261008.5:p.Ser174=
ENST00000409219.5:c.520T= ENSP00000386611.1:p.Ser174=
ENST00000409323.1:c.520T= ENSP00000386684.1:p.Ser174=
ENST00000409542.5:c.274T= ENSP00000387026.1:p.Ser92=
ENST00000435083.5:c.*164T= ENSP00000395805.1:n.*164T=
NM_000079.3:c.520T= NP_000070.1:p.Ser174=
NM_001039523.2:c.595T= NP_001034612.1:p.Ser199=
XM_017003256.1:c.616T= XP_016858745.1:p.Ser206=
XM_017003257.1:c.541T= XP_016858746.1:p.Ser181=
NM_000079.4:c.520T= MANE Select NP_000070.1:p.Ser174=
NM_001039523.3:c.595T= NP_001034612.1:p.Ser199=