Canonical Allele Identifier: CA1278359134

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108908281T= , CM000664.2:g.108908281T= GRCh38
NC_000002.11:g.109524737T= , CM000664.1:g.109524737T= GRCh37
NC_000002.10:g.108891169T= NCBI36
NG_008257.1:g.86092A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258443.7:c.804-262A= (EDAR) MANE Select ENSP00000258443.2:n.804-262A=
ENST00000258443.6:c.804-262A= (EDAR) ENSP00000258443.2:n.804-262A=
ENST00000376651.1:c.900-262A= (EDAR) ENSP00000365839.1:n.900-262A=
ENST00000409271.5:c.900-262A= (EDAR) ENSP00000386371.1:n.900-262A=
NM_022336.3:c.804-262A= (EDAR) NP_071731.1:n.804-262A=
XM_006712204.1:c.900-262A= (EDAR) XP_006712267.1:n.900-262A=
XM_011510502.1:c.951-262A= (EDAR) XP_011508804.1:n.951-262A=
XM_011510503.1:c.855-262A= (EDAR) XP_011508805.1:n.855-262A=
XM_011510504.1:c.231-262A= (EDAR) XP_011508806.1:n.231-262A=
XM_011510502.2:c.1044-262A= (EDAR) XP_011508804.2:n.1044-262A=
XM_011510503.2:c.948-262A= (EDAR) XP_011508805.2:n.948-262A=
XM_017004623.2:c.8370+135235T= (RANBP2) XP_016860112.1:n.8370+135235T=
NM_022336.4:c.804-262A= (EDAR) MANE Select NP_071731.1:n.804-262A=