Canonical Allele Identifier: CA1278354382

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108897322_108897323delinsTG , CM000664.2:g.108897322_108897323delinsTG GRCh38
NC_000002.11:g.109513778_109513779delinsTG , CM000664.1:g.109513778_109513779delinsTG GRCh37
NC_000002.10:g.108880210_108880211delinsTG NCBI36
NG_008257.1:g.97050_97051delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000258443.7:c.1025-94_1025-93delinsCA (EDAR) MANE Select ENSP00000258443.2:n.1025-94_1025-93delinsCA
ENST00000258443.6:c.1025-94_1025-93delinsCA (EDAR) ENSP00000258443.2:n.1025-94_1025-93delinsCA
ENST00000376651.1:c.1121-94_1121-93delinsCA (EDAR) ENSP00000365839.1:n.1121-94_1121-93delinsCA
ENST00000409271.5:c.1121-94_1121-93delinsCA (EDAR) ENSP00000386371.1:n.1121-94_1121-93delinsCA
NM_022336.3:c.1025-94_1025-93delinsCA (EDAR) NP_071731.1:n.1025-94_1025-93delinsCA
XM_006712204.1:c.1121-94_1121-93delinsCA (EDAR) XP_006712267.1:n.1121-94_1121-93delinsCA
XM_011510502.1:c.1172-94_1172-93delinsCA (EDAR) XP_011508804.1:n.1172-94_1172-93delinsCA
XM_011510503.1:c.1076-94_1076-93delinsCA (EDAR) XP_011508805.1:n.1076-94_1076-93delinsCA
XM_011510504.1:c.452-94_452-93delinsCA (EDAR) XP_011508806.1:n.452-94_452-93delinsCA
XM_011510502.2:c.1265-94_1265-93delinsCA (EDAR) XP_011508804.2:n.1265-94_1265-93delinsCA
XM_011510503.2:c.1169-94_1169-93delinsCA (EDAR) XP_011508805.2:n.1169-94_1169-93delinsCA
XM_017004623.2:c.8370+124276_8370+124277delinsTG (RANBP2) XP_016860112.1:n.8370+124276_8370+124277delinsTG
NM_022336.4:c.1025-94_1025-93delinsCA (EDAR) MANE Select NP_071731.1:n.1025-94_1025-93delinsCA