Canonical Allele Identifier: CA2577065513

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108897329_108897330del , CM000664.2:g.108897329_108897330del GRCh38
NC_000002.11:g.109513785_109513786del , CM000664.1:g.109513785_109513786del GRCh37
NC_000002.10:g.108880217_108880218del NCBI36
NG_008257.1:g.97048_97049del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258443.7:c.1025-96_1025-95del (EDAR) MANE Select ENSP00000258443.2:n.1025-96_1025-95del
ENST00000258443.6:c.1025-96_1025-95del (EDAR) ENSP00000258443.2:n.1025-96_1025-95del
ENST00000376651.1:c.1121-96_1121-95del (EDAR) ENSP00000365839.1:n.1121-96_1121-95del
ENST00000409271.5:c.1121-96_1121-95del (EDAR) ENSP00000386371.1:n.1121-96_1121-95del
NM_022336.3:c.1025-96_1025-95del (EDAR) NP_071731.1:n.1025-96_1025-95del
XM_006712204.1:c.1121-96_1121-95del (EDAR) XP_006712267.1:n.1121-96_1121-95del
XM_011510502.1:c.1172-96_1172-95del (EDAR) XP_011508804.1:n.1172-96_1172-95del
XM_011510503.1:c.1076-96_1076-95del (EDAR) XP_011508805.1:n.1076-96_1076-95del
XM_011510504.1:c.452-96_452-95del (EDAR) XP_011508806.1:n.452-96_452-95del
XM_011510502.2:c.1265-96_1265-95del (EDAR) XP_011508804.2:n.1265-96_1265-95del
XM_011510503.2:c.1169-96_1169-95del (EDAR) XP_011508805.2:n.1169-96_1169-95del
XM_017004623.2:c.8370+124283_8370+124284del (RANBP2) XP_016860112.1:n.8370+124283_8370+124284del
NM_022336.4:c.1025-96_1025-95del (EDAR) MANE Select NP_071731.1:n.1025-96_1025-95del