Canonical Allele Identifier: CA1974358
Community Standard Title: NM_000079.4(CHRNA1):c.1143C>T (p.Gly381=)
Gene: CHRNA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.174748679G>A , CM000664.2:g.174748679G>A GRCh38
NC_000002.11:g.175613407G>A , CM000664.1:g.175613407G>A GRCh37
NC_000002.10:g.175321653G>A NCBI36
NG_008172.1:g.20794C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000079.4:c.1143C>T MANE Select NP_000070.1:p.Gly381=
ENST00000348749.9:c.1143C>T MANE Select ENSP00000261008.5:p.Gly381=
NM_000079.3:c.1143C>T NP_000070.1:p.Gly381=
NM_001039523.2:c.1218C>T NP_001034612.1:p.Gly406=
NM_001039523.3:c.1218C>T NP_001034612.1:p.Gly406=
ENST00000261007.9:c.1218C>T ENSP00000261007.5:p.Gly406=
ENST00000409219.5:c.1003-424C>T ENSP00000386611.1:n.1003-424C>T
ENST00000409542.5:c.897C>T ENSP00000387026.1:p.Gly299=
ENST00000435083.5:c.*787C>T ENSP00000395805.1:n.*787C>T
ENST00000636168.2:c.654C>T ENSP00000490338.2:p.Gly218=
ENST00000672640.1:c.654C>T ENSP00000500507.1:p.Gly218=
XM_017003256.1:c.1239C>T XP_016858745.1:p.Gly413=
XM_017003257.1:c.1164C>T XP_016858746.1:p.Gly388=