Canonical Allele Identifier: CA2842597658

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108959289A>G , CM000664.2:g.108959289A>G GRCh38
NC_000002.11:g.109575745A>G , CM000664.1:g.109575745A>G GRCh37
NC_000002.10:g.108942177A>G NCBI36
NG_008257.1:g.35084T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258443.7:c.-18-28257T>C (EDAR) MANE Select ENSP00000258443.2:n.-18-28257T>C
ENST00000258443.6:c.-18-28257T>C (EDAR) ENSP00000258443.2:n.-18-28257T>C
ENST00000376651.1:c.-18-28257T>C (EDAR) ENSP00000365839.1:n.-18-28257T>C
ENST00000409271.5:c.-134-18963T>C (EDAR) ENSP00000386371.1:n.-134-18963T>C
NM_022336.3:c.-18-28257T>C (EDAR) NP_071731.1:n.-18-28257T>C
XM_006712204.1:c.-18-28257T>C (EDAR) XP_006712267.1:n.-18-28257T>C
XM_011510502.1:c.33+6334T>C (EDAR) XP_011508804.1:n.33+6334T>C
XM_011510503.1:c.33+6334T>C (EDAR) XP_011508805.1:n.33+6334T>C
XM_011510502.2:c.126+6334T>C (EDAR) XP_011508804.2:n.126+6334T>C
XM_011510503.2:c.126+6334T>C (EDAR) XP_011508805.2:n.126+6334T>C
XM_017004623.2:c.8370+186243A>G (RANBP2) XP_016860112.1:n.8370+186243A>G
NM_022336.4:c.-18-28257T>C (EDAR) MANE Select NP_071731.1:n.-18-28257T>C