Canonical Allele Identifier: CA348051146

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108908008G>C , CM000664.2:g.108908008G>C GRCh38
NC_000002.11:g.109524464G>C , CM000664.1:g.109524464G>C GRCh37
NC_000002.10:g.108890896G>C NCBI36
NG_008257.1:g.86365C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258443.7:c.815C>G (EDAR) MANE Select ENSP00000258443.2:p.Ala272Gly
ENST00000258443.6:c.815C>G (EDAR) ENSP00000258443.2:p.Ala272Gly
ENST00000376651.1:c.911C>G (EDAR) ENSP00000365839.1:p.Ala304Gly
ENST00000409271.5:c.911C>G (EDAR) ENSP00000386371.1:p.Ala304Gly
NM_022336.3:c.815C>G (EDAR) NP_071731.1:p.Ala272Gly
XM_006712204.1:c.911C>G (EDAR) XP_006712267.1:p.Ala304Gly
XM_011510502.1:c.962C>G (EDAR) XP_011508804.1:p.Ala321Gly
XM_011510503.1:c.866C>G (EDAR) XP_011508805.1:p.Ala289Gly
XM_011510504.1:c.242C>G (EDAR) XP_011508806.1:p.Ala81Gly
XM_011510502.2:c.1055C>G (EDAR) XP_011508804.2:p.Ala352Gly
XM_011510503.2:c.959C>G (EDAR) XP_011508805.2:p.Ala320Gly
XM_017004623.2:c.8370+134962G>C (RANBP2) XP_016860112.1:n.8370+134962G>C
NM_022336.4:c.815C>G (EDAR) MANE Select NP_071731.1:p.Ala272Gly