Canonical Allele Identifier: CA348047834

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108897014T>C , CM000664.2:g.108897014T>C GRCh38
NC_000002.11:g.109513470T>C , CM000664.1:g.109513470T>C GRCh37
NC_000002.10:g.108879902T>C NCBI36
NG_008257.1:g.97359A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258443.7:c.1240A>G (EDAR) MANE Select ENSP00000258443.2:p.Lys414Glu
ENST00000258443.6:c.1240A>G (EDAR) ENSP00000258443.2:p.Lys414Glu
ENST00000376651.1:c.1336A>G (EDAR) ENSP00000365839.1:p.Lys446Glu
ENST00000409271.5:c.1336A>G (EDAR) ENSP00000386371.1:p.Lys446Glu
NM_022336.3:c.1240A>G (EDAR) NP_071731.1:p.Lys414Glu
XM_006712204.1:c.1336A>G (EDAR) XP_006712267.1:p.Lys446Glu
XM_011510502.1:c.1387A>G (EDAR) XP_011508804.1:p.Lys463Glu
XM_011510503.1:c.1291A>G (EDAR) XP_011508805.1:p.Lys431Glu
XM_011510504.1:c.667A>G (EDAR) XP_011508806.1:p.Lys223Glu
XM_011510502.2:c.1480A>G (EDAR) XP_011508804.2:p.Lys494Glu
XM_011510503.2:c.1384A>G (EDAR) XP_011508805.2:p.Lys462Glu
XM_017004623.2:c.8370+123968T>C (RANBP2) XP_016860112.1:n.8370+123968T>C
NM_022336.4:c.1240A>G (EDAR) MANE Select NP_071731.1:p.Lys414Glu