Canonical Allele Identifier: CA2838374095
Gene: EDARADD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236427446dup , CM000663.2:g.236427446dup GRCh38
NC_000001.10:g.236590746dup , CM000663.1:g.236590746dup GRCh37
NC_000001.9:g.234657369dup NCBI36
NG_011566.1:g.38067dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000334232.9:c.215dup MANE Select ENSP00000335076.4:p.Asn72LysfsTer11
ENST00000359362.6:c.185dup ENSP00000352320.4:p.Asn62LysfsTer11
ENST00000637660.1:c.149dup ENSP00000490347.1:p.Asn50LysfsTer11
ENST00000642595.1:c.185dup ENSP00000494458.1:p.Asn62LysfsTer11
ENST00000334232.8:c.215dup ENSP00000335076.4:p.Asn72LysfsTer11
ENST00000359362.5:c.185dup ENSP00000352320.4:p.Asn62LysfsTer11
ENST00000439430.5:c.149dup ENSP00000405815.1:p.Asn50LysfsTer11
NM_080738.3:c.185dup NP_542776.1:p.Asn62LysfsTer11
NM_145861.2:c.215dup NP_665860.2:p.Asn72LysfsTer11
NM_080738.4:c.185dup NP_542776.1:p.Asn62LysfsTer11
NM_145861.4:c.215dup MANE Select NP_665860.2:p.Asn72LysfsTer11