Canonical Allele Identifier: CA636613729
Gene: CHRNA4 HGNC NCBI

Linked Data

dbSNP Id: rs1464175973

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350759_63350760insAAAAAAAAAAA , CM000682.2:g.63350759_63350760insAAAAAAAAAAA GRCh38
NC_000020.10:g.61982111_61982112insAAAAAAAAAAA , CM000682.1:g.61982111_61982112insAAAAAAAAAAA GRCh37
NC_000020.9:g.61452555_61452556insAAAAAAAAAAA NCBI36
NG_011931.1:g.15585_15586insTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000370263.9:c.652_653insTTTTTTTTTTT MANE Select ENSP00000359285.4:p.Tyr218PhefsTer?
ENST00000370263.8:c.652_653insTTTTTTTTTTT ENSP00000359285.4:p.Tyr218PhefsTer?
ENST00000463705.5:n.1300_1301insTTTTTTTTTTT
ENST00000467563.3:n.722_723insTTTTTTTTTTT
ENST00000498043.6:c.676_677insTTTTTTTTTTT
ENST00000615287.4:c.439_440insTTTTTTTTTTT ENSP00000483388.1:p.Tyr147PhefsTer?
ENST00000627000.1:c.*341_*342insTTTTTTTTTTT ENSP00000486914.1:n.*341_*342insTTTTTTTTTTT
ENST00000630240.1:n.373_374insTTTTTTTTTTT
NM_000744.6:c.652_653insTTTTTTTTTTT NP_000735.1:p.Tyr218PhefsTer?
NM_001256573.1:c.124_125insTTTTTTTTTTT NP_001243502.1:p.Tyr42PhefsTer?
NR_046317.1:n.908_909insTTTTTTTTTTT
XM_011528524.1:c.439_440insTTTTTTTTTTT XP_011526826.1:p.Tyr147PhefsTer?
XM_017027625.2:c.124_125insTTTTTTTTTTT XP_016883114.1:p.Tyr42PhefsTer?
XM_024451822.1:c.124_125insTTTTTTTTTTT XP_024307590.1:p.Tyr42PhefsTer?
NM_001256573.2:c.124_125insTTTTTTTTTTT NP_001243502.1:p.Tyr42PhefsTer?
NR_046317.2:n.861_862insTTTTTTTTTTT
NM_000744.7:c.652_653insTTTTTTTTTTT MANE Select NP_000735.1:p.Tyr218PhefsTer?