Canonical Allele Identifier: CA1278354347

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108897254A= , CM000664.2:g.108897254A= GRCh38
NC_000002.11:g.109513710A= , CM000664.1:g.109513710A= GRCh37
NC_000002.10:g.108880142A= NCBI36
NG_008257.1:g.97119T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258443.7:c.1025-25T= (EDAR) MANE Select ENSP00000258443.2:n.1025-25T=
ENST00000258443.6:c.1025-25T= (EDAR) ENSP00000258443.2:n.1025-25T=
ENST00000376651.1:c.1121-25T= (EDAR) ENSP00000365839.1:n.1121-25T=
ENST00000409271.5:c.1121-25T= (EDAR) ENSP00000386371.1:n.1121-25T=
NM_022336.3:c.1025-25T= (EDAR) NP_071731.1:n.1025-25T=
XM_006712204.1:c.1121-25T= (EDAR) XP_006712267.1:n.1121-25T=
XM_011510502.1:c.1172-25T= (EDAR) XP_011508804.1:n.1172-25T=
XM_011510503.1:c.1076-25T= (EDAR) XP_011508805.1:n.1076-25T=
XM_011510504.1:c.452-25T= (EDAR) XP_011508806.1:n.452-25T=
XM_011510502.2:c.1265-25T= (EDAR) XP_011508804.2:n.1265-25T=
XM_011510503.2:c.1169-25T= (EDAR) XP_011508805.2:n.1169-25T=
XM_017004623.2:c.8370+124208A= (RANBP2) XP_016860112.1:n.8370+124208A=
NM_022336.4:c.1025-25T= (EDAR) MANE Select NP_071731.1:n.1025-25T=