Canonical Allele Identifier: CA1308832525
Gene: CHRNA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.174750005_174750014delinsCGATGACAGT , CM000664.2:g.174750005_174750014delinsCGATGACAGT GRCh38
NC_000002.11:g.175614733_175614742delinsCGATGACAGT , CM000664.1:g.175614733_175614742delinsCGATGACAGT GRCh37
NC_000002.10:g.175322979_175322988delinsCGATGACAGT NCBI36
NG_008172.1:g.19459_19468delinsACTGTCATCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000636168.2:c.445_454delinsACTGTCATCG ENSP00000490338.2:p.Thr149=
ENST00000672640.1:c.445_454delinsACTGTCATCG ENSP00000500507.1:p.Thr149=
ENST00000261007.9:c.1009_1018delinsACTGTCATCG ENSP00000261007.5:p.Thr337=
ENST00000348749.9:c.934_943delinsACTGTCATCG MANE Select ENSP00000261008.5:p.Thr312=
ENST00000409219.5:c.934_943delinsACTGTCATCG ENSP00000386611.1:p.Thr312=
ENST00000409542.5:c.688_697delinsACTGTCATCG ENSP00000387026.1:p.Thr230=
ENST00000435083.5:c.*578_*587delinsACTGTCATCG ENSP00000395805.1:n.*578_*587delinsACTGTCATCG
NM_000079.3:c.934_943delinsACTGTCATCG NP_000070.1:p.Thr312=
NM_001039523.2:c.1009_1018delinsACTGTCATCG NP_001034612.1:p.Thr337=
XM_017003256.1:c.1030_1039delinsACTGTCATCG XP_016858745.1:p.Thr344=
XM_017003257.1:c.955_964delinsACTGTCATCG XP_016858746.1:p.Thr319=
NM_000079.4:c.934_943delinsACTGTCATCG MANE Select NP_000070.1:p.Thr312=
NM_001039523.3:c.1009_1018delinsACTGTCATCG NP_001034612.1:p.Thr337=