Canonical Allele Identifier: CA2374743257
Community Standard Title: NM_000744.7(CHRNA4):c.442C= (p.Arg148=)
Gene: CHRNA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350969G= , CM000682.2:g.63350969G= GRCh38
NC_000020.10:g.61982321G= , CM000682.1:g.61982321G= GRCh37
NC_000020.9:g.61452765G= NCBI36
NG_011931.1:g.15375C=

Transcript Alleles

HGVS Amino-acid Change
NM_000744.7:c.442C= MANE Select NP_000735.1:p.Arg148=
ENST00000370263.9:c.442C= MANE Select ENSP00000359285.4:p.Arg148=
NM_000744.6:c.442C= NP_000735.1:p.Arg148=
NM_001256573.1:c.-87C= NP_001243502.1:n.-87C=
NM_001256573.2:c.-87C= NP_001243502.1:n.-87C=
NR_046317.1:n.698C=
NR_046317.2:n.651C=
ENST00000370263.8:c.442C= ENSP00000359285.4:p.Arg148=
ENST00000463705.5:n.1090C=
ENST00000467563.3:n.512C=
ENST00000498043.6:c.466C=
ENST00000615287.4:c.229C= ENSP00000483388.1:p.Arg77=
ENST00000627000.1:c.*131C= ENSP00000486914.1:n.*131C=
ENST00000628665.1:n.485C=
ENST00000630240.1:n.163C=
XM_011528524.1:c.229C= XP_011526826.1:p.Arg77=
XM_017027625.2:c.-87C= XP_016883114.1:n.-87C=
XM_024451822.1:c.-87C= XP_024307590.1:n.-87C=