Canonical Allele Identifier: CA1278368604

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108929383T= , CM000664.2:g.108929383T= GRCh38
NC_000002.11:g.109545839T= , CM000664.1:g.109545839T= GRCh37
NC_000002.10:g.108912271T= NCBI36
NG_008257.1:g.64990A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258443.7:c.175-4A= (EDAR) MANE Select ENSP00000258443.2:n.175-4A=
ENST00000258443.6:c.175-4A= (EDAR) ENSP00000258443.2:n.175-4A=
ENST00000376651.1:c.175-4A= (EDAR) ENSP00000365839.1:n.175-4A=
ENST00000409271.5:c.175-4A= (EDAR) ENSP00000386371.1:n.175-4A=
NM_022336.3:c.175-4A= (EDAR) NP_071731.1:n.175-4A=
XM_006712204.1:c.175-4A= (EDAR) XP_006712267.1:n.175-4A=
XM_011510502.1:c.226-4A= (EDAR) XP_011508804.1:n.226-4A=
XM_011510503.1:c.226-4A= (EDAR) XP_011508805.1:n.226-4A=
XM_011510502.2:c.319-4A= (EDAR) XP_011508804.2:n.319-4A=
XM_011510503.2:c.319-4A= (EDAR) XP_011508805.2:n.319-4A=
XM_017004623.2:c.8370+156337T= (RANBP2) XP_016860112.1:n.8370+156337T=
NM_022336.4:c.175-4A= (EDAR) MANE Select NP_071731.1:n.175-4A=