Canonical Allele Identifier: CA2374743203
Gene: CHRNA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350859G= , CM000682.2:g.63350859G= GRCh38
NC_000020.10:g.61982211G= , CM000682.1:g.61982211G= GRCh37
NC_000020.9:g.61452655G= NCBI36
NG_011931.1:g.15485C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370263.9:c.552C= MANE Select ENSP00000359285.4:p.Tyr184=
ENST00000370263.8:c.552C= ENSP00000359285.4:p.Tyr184=
ENST00000463705.5:n.1200C=
ENST00000467563.3:n.622C=
ENST00000498043.6:c.576C=
ENST00000615287.4:c.339C= ENSP00000483388.1:p.Tyr113=
ENST00000627000.1:c.*241C= ENSP00000486914.1:n.*241C=
ENST00000630240.1:n.273C=
NM_000744.6:c.552C= NP_000735.1:p.Tyr184=
NM_001256573.1:c.24C= NP_001243502.1:p.Tyr8=
NR_046317.1:n.808C=
XM_011528524.1:c.339C= XP_011526826.1:p.Tyr113=
XM_017027625.2:c.24C= XP_016883114.1:p.Tyr8=
XM_024451822.1:c.24C= XP_024307590.1:p.Tyr8=
NM_001256573.2:c.24C= NP_001243502.1:p.Tyr8=
NR_046317.2:n.761C=
NM_000744.7:c.552C= MANE Select NP_000735.1:p.Tyr184=