Canonical Allele Identifier: CA2486933361
Gene: EDARADD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236482306G= , CM000663.2:g.236482306G= GRCh38
NC_000001.10:g.236645606G= , CM000663.1:g.236645606G= GRCh37
NC_000001.9:g.234712229G= NCBI36
NG_011566.1:g.92927G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334232.9:c.305G= MANE Select ENSP00000335076.4:p.Cys102=
ENST00000359362.6:c.275G= ENSP00000352320.4:p.Cys92=
ENST00000637660.1:c.239G= ENSP00000490347.1:p.Cys80=
ENST00000642595.1:c.236-9431G= ENSP00000494458.1:n.236-9431G=
ENST00000334232.8:c.305G= ENSP00000335076.4:p.Cys102=
ENST00000359362.5:c.275G= ENSP00000352320.4:p.Cys92=
ENST00000439430.5:c.239G= ENSP00000405815.1:p.Cys80=
NM_080738.3:c.275G= NP_542776.1:p.Cys92=
NM_145861.2:c.305G= NP_665860.2:p.Cys102=
NM_080738.4:c.275G= NP_542776.1:p.Cys92=
NM_145861.4:c.305G= MANE Select NP_665860.2:p.Cys102=