Canonical Allele Identifier: CA1278354291

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108897131G= , CM000664.2:g.108897131G= GRCh38
NC_000002.11:g.109513587G= , CM000664.1:g.109513587G= GRCh37
NC_000002.10:g.108880019G= NCBI36
NG_008257.1:g.97242C=

Transcript Alleles

HGVS Amino-acid change
ENST00000258443.7:c.1123C= (EDAR) MANE Select ENSP00000258443.2:p.Arg375=
ENST00000258443.6:c.1123C= (EDAR) ENSP00000258443.2:p.Arg375=
ENST00000376651.1:c.1219C= (EDAR) ENSP00000365839.1:p.Arg407=
ENST00000409271.5:c.1219C= (EDAR) ENSP00000386371.1:p.Arg407=
NM_022336.3:c.1123C= (EDAR) NP_071731.1:p.Arg375=
XM_006712204.1:c.1219C= (EDAR) XP_006712267.1:p.Arg407=
XM_011510502.1:c.1270C= (EDAR) XP_011508804.1:p.Arg424=
XM_011510503.1:c.1174C= (EDAR) XP_011508805.1:p.Arg392=
XM_011510504.1:c.550C= (EDAR) XP_011508806.1:p.Arg184=
XM_011510502.2:c.1363C= (EDAR) XP_011508804.2:p.Arg455=
XM_011510503.2:c.1267C= (EDAR) XP_011508805.2:p.Arg423=
XM_017004623.2:c.8370+124085G= (RANBP2) XP_016860112.1:n.8370+124085G=
NM_022336.4:c.1123C= (EDAR) MANE Select NP_071731.1:p.Arg375=