Canonical Allele Identifier: CA2486933363
Gene: EDARADD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236482311T= , CM000663.2:g.236482311T= GRCh38
NC_000001.10:g.236645611T= , CM000663.1:g.236645611T= GRCh37
NC_000001.9:g.234712234T= NCBI36
NG_011566.1:g.92932T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334232.9:c.310T= MANE Select ENSP00000335076.4:p.Ser104=
ENST00000359362.6:c.280T= ENSP00000352320.4:p.Ser94=
ENST00000637660.1:c.244T= ENSP00000490347.1:p.Ser82=
ENST00000642595.1:c.236-9426T= ENSP00000494458.1:n.236-9426T=
ENST00000334232.8:c.310T= ENSP00000335076.4:p.Ser104=
ENST00000359362.5:c.280T= ENSP00000352320.4:p.Ser94=
ENST00000439430.5:c.244T= ENSP00000405815.1:p.Ser82=
NM_080738.3:c.280T= NP_542776.1:p.Ser94=
NM_145861.2:c.310T= NP_665860.2:p.Ser104=
NM_080738.4:c.280T= NP_542776.1:p.Ser94=
NM_145861.4:c.310T= MANE Select NP_665860.2:p.Ser104=