Canonical Allele Identifier: CA348115853

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108929348T>A , CM000664.2:g.108929348T>A GRCh38
NC_000002.11:g.109545804T>A , CM000664.1:g.109545804T>A GRCh37
NC_000002.10:g.108912236T>A NCBI36
NG_008257.1:g.65025A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000258443.7:c.206A>T (EDAR) MANE Select ENSP00000258443.2:p.Tyr69Phe
ENST00000258443.6:c.206A>T (EDAR) ENSP00000258443.2:p.Tyr69Phe
ENST00000376651.1:c.206A>T (EDAR) ENSP00000365839.1:p.Tyr69Phe
ENST00000409271.5:c.206A>T (EDAR) ENSP00000386371.1:p.Tyr69Phe
NM_022336.3:c.206A>T (EDAR) NP_071731.1:p.Tyr69Phe
XM_006712204.1:c.206A>T (EDAR) XP_006712267.1:p.Tyr69Phe
XM_011510502.1:c.257A>T (EDAR) XP_011508804.1:p.Tyr86Phe
XM_011510503.1:c.257A>T (EDAR) XP_011508805.1:p.Tyr86Phe
XM_011510502.2:c.350A>T (EDAR) XP_011508804.2:p.Tyr117Phe
XM_011510503.2:c.350A>T (EDAR) XP_011508805.2:p.Tyr117Phe
XM_017004623.2:c.8370+156302T>A (RANBP2) XP_016860112.1:n.8370+156302T>A
NM_022336.4:c.206A>T (EDAR) MANE Select NP_071731.1:p.Tyr69Phe