Canonical Allele Identifier: CA2486933397
Gene: EDARADD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236482405C= , CM000663.2:g.236482405C= GRCh38
NC_000001.10:g.236645705C= , CM000663.1:g.236645705C= GRCh37
NC_000001.9:g.234712328C= NCBI36
NG_011566.1:g.93026C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334232.9:c.404C= MANE Select ENSP00000335076.4:p.Thr135=
ENST00000359362.6:c.374C= ENSP00000352320.4:p.Thr125=
ENST00000637660.1:c.338C= ENSP00000490347.1:p.Thr113=
ENST00000642595.1:c.236-9332C= ENSP00000494458.1:n.236-9332C=
ENST00000334232.8:c.404C= ENSP00000335076.4:p.Thr135=
ENST00000359362.5:c.374C= ENSP00000352320.4:p.Thr125=
NM_080738.3:c.374C= NP_542776.1:p.Thr125=
NM_145861.2:c.404C= NP_665860.2:p.Thr135=
NM_080738.4:c.374C= NP_542776.1:p.Thr125=
NM_145861.4:c.404C= MANE Select NP_665860.2:p.Thr135=