Canonical Allele Identifier: CA1278354264

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108897084_108897085delinsGC , CM000664.2:g.108897084_108897085delinsGC GRCh38
NC_000002.11:g.109513540_109513541delinsGC , CM000664.1:g.109513540_109513541delinsGC GRCh37
NC_000002.10:g.108879972_108879973delinsGC NCBI36
NG_008257.1:g.97288_97289delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000258443.7:c.1169_1170delinsGC (EDAR) MANE Select ENSP00000258443.2:p.Gly390=
ENST00000258443.6:c.1169_1170delinsGC (EDAR) ENSP00000258443.2:p.Gly390=
ENST00000376651.1:c.1265_1266delinsGC (EDAR) ENSP00000365839.1:p.Gly422=
ENST00000409271.5:c.1265_1266delinsGC (EDAR) ENSP00000386371.1:p.Gly422=
NM_022336.3:c.1169_1170delinsGC (EDAR) NP_071731.1:p.Gly390=
XM_006712204.1:c.1265_1266delinsGC (EDAR) XP_006712267.1:p.Gly422=
XM_011510502.1:c.1316_1317delinsGC (EDAR) XP_011508804.1:p.Gly439=
XM_011510503.1:c.1220_1221delinsGC (EDAR) XP_011508805.1:p.Gly407=
XM_011510504.1:c.596_597delinsGC (EDAR) XP_011508806.1:p.Gly199=
XM_011510502.2:c.1409_1410delinsGC (EDAR) XP_011508804.2:p.Gly470=
XM_011510503.2:c.1313_1314delinsGC (EDAR) XP_011508805.2:p.Gly438=
XM_017004623.2:c.8370+124038_8370+124039delinsGC (RANBP2) XP_016860112.1:n.8370+124038_8370+124039delinsGC
NM_022336.4:c.1169_1170delinsGC (EDAR) MANE Select NP_071731.1:p.Gly390=