Canonical Allele Identifier: CA1278354357

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108897274A= , CM000664.2:g.108897274A= GRCh38
NC_000002.11:g.109513730A= , CM000664.1:g.109513730A= GRCh37
NC_000002.10:g.108880162A= NCBI36
NG_008257.1:g.97099T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258443.7:c.1025-45T= (EDAR) MANE Select ENSP00000258443.2:n.1025-45T=
ENST00000258443.6:c.1025-45T= (EDAR) ENSP00000258443.2:n.1025-45T=
ENST00000376651.1:c.1121-45T= (EDAR) ENSP00000365839.1:n.1121-45T=
ENST00000409271.5:c.1121-45T= (EDAR) ENSP00000386371.1:n.1121-45T=
NM_022336.3:c.1025-45T= (EDAR) NP_071731.1:n.1025-45T=
XM_006712204.1:c.1121-45T= (EDAR) XP_006712267.1:n.1121-45T=
XM_011510502.1:c.1172-45T= (EDAR) XP_011508804.1:n.1172-45T=
XM_011510503.1:c.1076-45T= (EDAR) XP_011508805.1:n.1076-45T=
XM_011510504.1:c.452-45T= (EDAR) XP_011508806.1:n.452-45T=
XM_011510502.2:c.1265-45T= (EDAR) XP_011508804.2:n.1265-45T=
XM_011510503.2:c.1169-45T= (EDAR) XP_011508805.2:n.1169-45T=
XM_017004623.2:c.8370+124228A= (RANBP2) XP_016860112.1:n.8370+124228A=
NM_022336.4:c.1025-45T= (EDAR) MANE Select NP_071731.1:n.1025-45T=