Canonical Allele Identifier: CA2586969751

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108929199_108929380del , CM000664.2:g.108929199_108929380del GRCh38
NC_000002.11:g.109545655_109545836del , CM000664.1:g.109545655_109545836del GRCh37
NC_000002.10:g.108912087_108912268del NCBI36
NG_008257.1:g.64994_65175del

Transcript Alleles

HGVS Amino-acid change
ENST00000258443.7:c.175_356del (EDAR)
ENST00000258443.6:c.175_356del (EDAR)
ENST00000376651.1:c.175_356del (EDAR)
ENST00000409271.5:c.175_356del (EDAR)
NM_022336.3:c.175_356del (EDAR)
XM_006712204.1:c.175_356del (EDAR)
XM_011510502.1:c.226_407del (EDAR)
XM_011510503.1:c.226_407del (EDAR)
XM_011510502.2:c.319_500del (EDAR)
XM_011510503.2:c.319_500del (EDAR)
XM_017004623.2:c.8370+156153_8370+156334del (RANBP2) XP_016860112.1:n.8370+156153_8370+156334d...
NM_022336.4:c.175_356del (EDAR)