Canonical Allele Identifier: CA2486933359
Gene: EDARADD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236482303C= , CM000663.2:g.236482303C= GRCh38
NC_000001.10:g.236645603C= , CM000663.1:g.236645603C= GRCh37
NC_000001.9:g.234712226C= NCBI36
NG_011566.1:g.92924C=

Transcript Alleles

HGVS Amino-acid change
ENST00000334232.9:c.302C= MANE Select ENSP00000335076.4:p.Thr101=
ENST00000359362.6:c.272C= ENSP00000352320.4:p.Thr91=
ENST00000637660.1:c.236C= ENSP00000490347.1:p.Thr79=
ENST00000642595.1:c.236-9434C= ENSP00000494458.1:n.236-9434C=
ENST00000334232.8:c.302C= ENSP00000335076.4:p.Thr101=
ENST00000359362.5:c.272C= ENSP00000352320.4:p.Thr91=
ENST00000439430.5:c.236C= ENSP00000405815.1:p.Thr79=
NM_080738.3:c.272C= NP_542776.1:p.Thr91=
NM_145861.2:c.302C= NP_665860.2:p.Thr101=
NM_080738.4:c.272C= NP_542776.1:p.Thr91=
NM_145861.4:c.302C= MANE Select NP_665860.2:p.Thr101=