Canonical Allele Identifier: CA1824895

Linked Data

dbSNP Id: rs761615482

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108907933G>A , CM000664.2:g.108907933G>A GRCh38
NC_000002.11:g.109524389G>A , CM000664.1:g.109524389G>A GRCh37
NC_000002.10:g.108890821G>A NCBI36
NG_008257.1:g.86440C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258443.7:c.890C>T (EDAR) MANE Select ENSP00000258443.2:p.Ser297Phe
ENST00000258443.6:c.890C>T (EDAR) ENSP00000258443.2:p.Ser297Phe
ENST00000376651.1:c.986C>T (EDAR) ENSP00000365839.1:p.Ser329Phe
ENST00000409271.5:c.986C>T (EDAR) ENSP00000386371.1:p.Ser329Phe
NM_022336.3:c.890C>T (EDAR) NP_071731.1:p.Ser297Phe
XM_006712204.1:c.986C>T (EDAR) XP_006712267.1:p.Ser329Phe
XM_011510502.1:c.1037C>T (EDAR) XP_011508804.1:p.Ser346Phe
XM_011510503.1:c.941C>T (EDAR) XP_011508805.1:p.Ser314Phe
XM_011510504.1:c.317C>T (EDAR) XP_011508806.1:p.Ser106Phe
XM_011510502.2:c.1130C>T (EDAR) XP_011508804.2:p.Ser377Phe
XM_011510503.2:c.1034C>T (EDAR) XP_011508805.2:p.Ser345Phe
XM_017004623.2:c.8370+134887G>A (RANBP2) XP_016860112.1:n.8370+134887G>A
NM_022336.4:c.890C>T (EDAR) MANE Select NP_071731.1:p.Ser297Phe