Canonical Allele Identifier: CA1278368508

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108929200A= , CM000664.2:g.108929200A= GRCh38
NC_000002.11:g.109545656A= , CM000664.1:g.109545656A= GRCh37
NC_000002.10:g.108912088A= NCBI36
NG_008257.1:g.65173T=

Transcript Alleles

HGVS Amino-acid change
ENST00000258443.7:c.354T= (EDAR) MANE Select ENSP00000258443.2:p.Pro118=
ENST00000258443.6:c.354T= (EDAR) ENSP00000258443.2:p.Pro118=
ENST00000376651.1:c.354T= (EDAR) ENSP00000365839.1:p.Pro118=
ENST00000409271.5:c.354T= (EDAR) ENSP00000386371.1:p.Pro118=
NM_022336.3:c.354T= (EDAR) NP_071731.1:p.Pro118=
XM_006712204.1:c.354T= (EDAR) XP_006712267.1:p.Pro118=
XM_011510502.1:c.405T= (EDAR) XP_011508804.1:p.Pro135=
XM_011510503.1:c.405T= (EDAR) XP_011508805.1:p.Pro135=
XM_011510502.2:c.498T= (EDAR) XP_011508804.2:p.Pro166=
XM_011510503.2:c.498T= (EDAR) XP_011508805.2:p.Pro166=
XM_017004623.2:c.8370+156154A= (RANBP2) XP_016860112.1:n.8370+156154A=
NM_022336.4:c.354T= (EDAR) MANE Select NP_071731.1:p.Pro118=