Canonical Allele Identifier: CA1974318
Gene: CHRNA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.174748250C>T , CM000664.2:g.174748250C>T GRCh38
NC_000002.11:g.175612978C>T , CM000664.1:g.175612978C>T GRCh37
NC_000002.10:g.175321224C>T NCBI36
NG_008172.1:g.21223G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000636168.2:c.759G>A ENSP00000490338.2:p.Ala253=
ENST00000672640.1:c.759G>A ENSP00000500507.1:p.Ala253=
ENST00000261007.9:c.1323G>A ENSP00000261007.5:p.Ala441=
ENST00000348749.9:c.1248G>A MANE Select ENSP00000261008.5:p.Ala416=
ENST00000409219.5:c.1008G>A ENSP00000386611.1:p.Ala336=
ENST00000409542.5:c.1002G>A ENSP00000387026.1:p.Ala334=
ENST00000435083.5:c.*892G>A ENSP00000395805.1:n.*892G>A
NM_000079.3:c.1248G>A NP_000070.1:p.Ala416=
NM_001039523.2:c.1323G>A NP_001034612.1:p.Ala441=
XM_017003256.1:c.1344G>A XP_016858745.1:p.Ala448=
XM_017003257.1:c.1269G>A XP_016858746.1:p.Ala423=
NM_000079.4:c.1248G>A MANE Select NP_000070.1:p.Ala416=
NM_001039523.3:c.1323G>A NP_001034612.1:p.Ala441=