Canonical Allele Identifier: CA1140886978
Gene: EDARADD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236482455G= , CM000663.2:g.236482455G= GRCh38
NC_000001.10:g.236645755G= , CM000663.1:g.236645755G= GRCh37
NC_000001.9:g.234712378G= NCBI36
NG_011566.1:g.93076G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334232.9:c.454G= MANE Select ENSP00000335076.4:p.Glu152=
ENST00000359362.6:c.424G= ENSP00000352320.4:p.Glu142=
ENST00000637660.1:c.388G= ENSP00000490347.1:p.Glu130=
ENST00000642595.1:c.236-9282G= ENSP00000494458.1:n.236-9282G=
ENST00000334232.8:c.454G= ENSP00000335076.4:p.Glu152=
ENST00000359362.5:c.424G= ENSP00000352320.4:p.Glu142=
NM_080738.3:c.424G= NP_542776.1:p.Glu142=
NM_145861.2:c.454G= NP_665860.2:p.Glu152=
NM_080738.4:c.424G= NP_542776.1:p.Glu142=
NM_145861.4:c.454G= MANE Select NP_665860.2:p.Glu152=