Canonical Allele Identifier: CA1278354403

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108897363_108897364delinsAC , CM000664.2:g.108897363_108897364delinsAC GRCh38
NC_000002.11:g.109513819_109513820delinsAC , CM000664.1:g.109513819_109513820delinsAC GRCh37
NC_000002.10:g.108880251_108880252delinsAC NCBI36
NG_008257.1:g.97009_97010delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000258443.7:c.1025-135_1025-134delinsGT (EDAR) MANE Select ENSP00000258443.2:n.1025-135_1025-134delinsGT
ENST00000258443.6:c.1025-135_1025-134delinsGT (EDAR) ENSP00000258443.2:n.1025-135_1025-134delinsGT
ENST00000376651.1:c.1121-135_1121-134delinsGT (EDAR) ENSP00000365839.1:n.1121-135_1121-134delinsGT
ENST00000409271.5:c.1121-135_1121-134delinsGT (EDAR) ENSP00000386371.1:n.1121-135_1121-134delinsGT
NM_022336.3:c.1025-135_1025-134delinsGT (EDAR) NP_071731.1:n.1025-135_1025-134delinsGT
XM_006712204.1:c.1121-135_1121-134delinsGT (EDAR) XP_006712267.1:n.1121-135_1121-134delinsGT
XM_011510502.1:c.1172-135_1172-134delinsGT (EDAR) XP_011508804.1:n.1172-135_1172-134delinsGT
XM_011510503.1:c.1076-135_1076-134delinsGT (EDAR) XP_011508805.1:n.1076-135_1076-134delinsGT
XM_011510504.1:c.452-135_452-134delinsGT (EDAR) XP_011508806.1:n.452-135_452-134delinsGT
XM_011510502.2:c.1265-135_1265-134delinsGT (EDAR) XP_011508804.2:n.1265-135_1265-134delinsGT
XM_011510503.2:c.1169-135_1169-134delinsGT (EDAR) XP_011508805.2:n.1169-135_1169-134delinsGT
XM_017004623.2:c.8370+124317_8370+124318delinsAC (RANBP2) XP_016860112.1:n.8370+124317_8370+124318delinsAC
NM_022336.4:c.1025-135_1025-134delinsGT (EDAR) MANE Select NP_071731.1:n.1025-135_1025-134delinsGT