Canonical Allele Identifier: CA2660592812

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108908061_108908063del , CM000664.2:g.108908061_108908063del GRCh38
NC_000002.11:g.109524517_109524519del , CM000664.1:g.109524517_109524519del GRCh37
NC_000002.10:g.108890949_108890951del NCBI36
NG_008257.1:g.86310_86312del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258443.7:c.804-44_804-42del (EDAR) MANE Select ENSP00000258443.2:n.804-44_804-42del
ENST00000258443.6:c.804-44_804-42del (EDAR) ENSP00000258443.2:n.804-44_804-42del
ENST00000376651.1:c.900-44_900-42del (EDAR) ENSP00000365839.1:n.900-44_900-42del
ENST00000409271.5:c.900-44_900-42del (EDAR) ENSP00000386371.1:n.900-44_900-42del
NM_022336.3:c.804-44_804-42del (EDAR) NP_071731.1:n.804-44_804-42del
XM_006712204.1:c.900-44_900-42del (EDAR) XP_006712267.1:n.900-44_900-42del
XM_011510502.1:c.951-44_951-42del (EDAR) XP_011508804.1:n.951-44_951-42del
XM_011510503.1:c.855-44_855-42del (EDAR) XP_011508805.1:n.855-44_855-42del
XM_011510504.1:c.231-44_231-42del (EDAR) XP_011508806.1:n.231-44_231-42del
XM_011510502.2:c.1044-44_1044-42del (EDAR) XP_011508804.2:n.1044-44_1044-42del
XM_011510503.2:c.948-44_948-42del (EDAR) XP_011508805.2:n.948-44_948-42del
XM_017004623.2:c.8370+135015_8370+135017del (RANBP2) XP_016860112.1:n.8370+135015_8370+135017del
NM_022336.4:c.804-44_804-42del (EDAR) MANE Select NP_071731.1:n.804-44_804-42del