Canonical Allele Identifier: CA345353497
Gene: EDARADD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236482312C>A , CM000663.2:g.236482312C>A GRCh38
NC_000001.10:g.236645612C>A , CM000663.1:g.236645612C>A GRCh37
NC_000001.9:g.234712235C>A NCBI36
NG_011566.1:g.92933C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000334232.9:c.311C>A MANE Select ENSP00000335076.4:p.Ser104Tyr
ENST00000359362.6:c.281C>A ENSP00000352320.4:p.Ser94Tyr
ENST00000637660.1:c.245C>A ENSP00000490347.1:p.Ser82Tyr
ENST00000642595.1:c.236-9425C>A ENSP00000494458.1:n.236-9425C>A
ENST00000334232.8:c.311C>A ENSP00000335076.4:p.Ser104Tyr
ENST00000359362.5:c.281C>A ENSP00000352320.4:p.Ser94Tyr
ENST00000439430.5:c.245C>A ENSP00000405815.1:p.Ser82Tyr
NM_080738.3:c.281C>A NP_542776.1:p.Ser94Tyr
NM_145861.2:c.311C>A NP_665860.2:p.Ser104Tyr
NM_080738.4:c.281C>A NP_542776.1:p.Ser94Tyr
NM_145861.4:c.311C>A MANE Select NP_665860.2:p.Ser104Tyr