Canonical Allele Identifier: CA2660593035

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108896729_108896732dup , CM000664.2:g.108896729_108896732dup GRCh38
NC_000002.11:g.109513185_109513188dup , CM000664.1:g.109513185_109513188dup GRCh37
NC_000002.10:g.108879617_108879620dup NCBI36
NG_008257.1:g.97642_97645dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000258443.7:c.*176_*179dup (EDAR) MANE Select ENSP00000258443.2:n.*176_*179dup
ENST00000258443.6:c.*176_*179dup (EDAR) ENSP00000258443.2:n.*176_*179dup
ENST00000376651.1:c.*176_*179dup (EDAR) ENSP00000365839.1:n.*176_*179dup
ENST00000409271.5:c.*176_*179dup (EDAR) ENSP00000386371.1:n.*176_*179dup
NM_022336.3:c.*176_*179dup (EDAR) NP_071731.1:n.*176_*179dup
XM_006712204.1:c.*176_*179dup (EDAR) XP_006712267.1:n.*176_*179dup
XM_011510502.1:c.*176_*179dup (EDAR) XP_011508804.1:n.*176_*179dup
XM_011510503.1:c.*176_*179dup (EDAR) XP_011508805.1:n.*176_*179dup
XM_011510504.1:c.*176_*179dup (EDAR) XP_011508806.1:n.*176_*179dup
XM_011510502.2:c.*176_*179dup (EDAR) XP_011508804.2:n.*176_*179dup
XM_011510503.2:c.*176_*179dup (EDAR) XP_011508805.2:n.*176_*179dup
XM_017004623.2:c.8370+123683_8370+123686dup (RANBP2) XP_016860112.1:n.8370+123683_8370+123686dup
NM_022336.4:c.*176_*179dup (EDAR) MANE Select NP_071731.1:n.*176_*179dup