Canonical Allele Identifier: CA1278368651

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108929460_108929461delinsTG , CM000664.2:g.108929460_108929461delinsTG GRCh38
NC_000002.11:g.109545916_109545917delinsTG , CM000664.1:g.109545916_109545917delinsTG GRCh37
NC_000002.10:g.108912348_108912349delinsTG NCBI36
NG_008257.1:g.64912_64913delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000258443.7:c.175-82_175-81delinsCA (EDAR) MANE Select ENSP00000258443.2:n.175-82_175-81delinsCA
ENST00000258443.6:c.175-82_175-81delinsCA (EDAR) ENSP00000258443.2:n.175-82_175-81delinsCA
ENST00000376651.1:c.175-82_175-81delinsCA (EDAR) ENSP00000365839.1:n.175-82_175-81delinsCA
ENST00000409271.5:c.175-82_175-81delinsCA (EDAR) ENSP00000386371.1:n.175-82_175-81delinsCA
NM_022336.3:c.175-82_175-81delinsCA (EDAR) NP_071731.1:n.175-82_175-81delinsCA
XM_006712204.1:c.175-82_175-81delinsCA (EDAR) XP_006712267.1:n.175-82_175-81delinsCA
XM_011510502.1:c.226-82_226-81delinsCA (EDAR) XP_011508804.1:n.226-82_226-81delinsCA
XM_011510503.1:c.226-82_226-81delinsCA (EDAR) XP_011508805.1:n.226-82_226-81delinsCA
XM_011510502.2:c.319-82_319-81delinsCA (EDAR) XP_011508804.2:n.319-82_319-81delinsCA
XM_011510503.2:c.319-82_319-81delinsCA (EDAR) XP_011508805.2:n.319-82_319-81delinsCA
XM_017004623.2:c.8370+156414_8370+156415delinsTG (RANBP2) XP_016860112.1:n.8370+156414_8370+156415delinsTG
NM_022336.4:c.175-82_175-81delinsCA (EDAR) MANE Select NP_071731.1:n.175-82_175-81delinsCA