Canonical Allele Identifier: CA2486933399
Gene: EDARADD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236482413A= , CM000663.2:g.236482413A= GRCh38
NC_000001.10:g.236645713A= , CM000663.1:g.236645713A= GRCh37
NC_000001.9:g.234712336A= NCBI36
NG_011566.1:g.93034A=

Transcript Alleles

HGVS Amino-acid change
ENST00000334232.9:c.412A= MANE Select ENSP00000335076.4:p.Asn138=
ENST00000359362.6:c.382A= ENSP00000352320.4:p.Asn128=
ENST00000637660.1:c.346A= ENSP00000490347.1:p.Asn116=
ENST00000642595.1:c.236-9324A= ENSP00000494458.1:n.236-9324A=
ENST00000334232.8:c.412A= ENSP00000335076.4:p.Asn138=
ENST00000359362.5:c.382A= ENSP00000352320.4:p.Asn128=
NM_080738.3:c.382A= NP_542776.1:p.Asn128=
NM_145861.2:c.412A= NP_665860.2:p.Asn138=
NM_080738.4:c.382A= NP_542776.1:p.Asn128=
NM_145861.4:c.412A= MANE Select NP_665860.2:p.Asn138=