Canonical Allele Identifier: CA348050966

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108907924A>T , CM000664.2:g.108907924A>T GRCh38
NC_000002.11:g.109524380A>T , CM000664.1:g.109524380A>T GRCh37
NC_000002.10:g.108890812A>T NCBI36
NG_008257.1:g.86449T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258443.7:c.899T>A (EDAR) MANE Select ENSP00000258443.2:p.Leu300Gln
ENST00000258443.6:c.899T>A (EDAR) ENSP00000258443.2:p.Leu300Gln
ENST00000376651.1:c.995T>A (EDAR) ENSP00000365839.1:p.Leu332Gln
ENST00000409271.5:c.995T>A (EDAR) ENSP00000386371.1:p.Leu332Gln
NM_022336.3:c.899T>A (EDAR) NP_071731.1:p.Leu300Gln
XM_006712204.1:c.995T>A (EDAR) XP_006712267.1:p.Leu332Gln
XM_011510502.1:c.1046T>A (EDAR) XP_011508804.1:p.Leu349Gln
XM_011510503.1:c.950T>A (EDAR) XP_011508805.1:p.Leu317Gln
XM_011510504.1:c.326T>A (EDAR) XP_011508806.1:p.Leu109Gln
XM_011510502.2:c.1139T>A (EDAR) XP_011508804.2:p.Leu380Gln
XM_011510503.2:c.1043T>A (EDAR) XP_011508805.2:p.Leu348Gln
XM_017004623.2:c.8370+134878A>T (RANBP2) XP_016860112.1:n.8370+134878A>T
NM_022336.4:c.899T>A (EDAR) MANE Select NP_071731.1:p.Leu300Gln