Canonical Allele Identifier: CA1278368586

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108929346_108929347delinsCG , CM000664.2:g.108929346_108929347delinsCG GRCh38
NC_000002.11:g.109545802_109545803delinsCG , CM000664.1:g.109545802_109545803delinsCG GRCh37
NC_000002.10:g.108912234_108912235delinsCG NCBI36
NG_008257.1:g.65026_65027delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000258443.7:c.207_208delinsCG (EDAR) MANE Select ENSP00000258443.2:p.Tyr69=
ENST00000258443.6:c.207_208delinsCG (EDAR) ENSP00000258443.2:p.Tyr69=
ENST00000376651.1:c.207_208delinsCG (EDAR) ENSP00000365839.1:p.Tyr69=
ENST00000409271.5:c.207_208delinsCG (EDAR) ENSP00000386371.1:p.Tyr69=
NM_022336.3:c.207_208delinsCG (EDAR) NP_071731.1:p.Tyr69=
XM_006712204.1:c.207_208delinsCG (EDAR) XP_006712267.1:p.Tyr69=
XM_011510502.1:c.258_259delinsCG (EDAR) XP_011508804.1:p.Tyr86=
XM_011510503.1:c.258_259delinsCG (EDAR) XP_011508805.1:p.Tyr86=
XM_011510502.2:c.351_352delinsCG (EDAR) XP_011508804.2:p.Tyr117=
XM_011510503.2:c.351_352delinsCG (EDAR) XP_011508805.2:p.Tyr117=
XM_017004623.2:c.8370+156300_8370+156301delinsCG (RANBP2) XP_016860112.1:n.8370+156300_8370+156301delinsCG
NM_022336.4:c.207_208delinsCG (EDAR) MANE Select NP_071731.1:p.Tyr69=