Canonical Allele Identifier: CA2660611278

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108929358_108929364del , CM000664.2:g.108929358_108929364del GRCh38
NC_000002.11:g.109545814_109545820del , CM000664.1:g.109545814_109545820del GRCh37
NC_000002.10:g.108912246_108912252del NCBI36
NG_008257.1:g.65011_65017del

Transcript Alleles

HGVS Amino-acid change
ENST00000258443.7:c.192_198del (EDAR) MANE Select ENSP00000258443.2:p.Lys65ArgfsTer?
ENST00000258443.6:c.192_198del (EDAR) ENSP00000258443.2:p.Lys65ArgfsTer?
ENST00000376651.1:c.192_198del (EDAR) ENSP00000365839.1:p.Lys65ArgfsTer?
ENST00000409271.5:c.192_198del (EDAR) ENSP00000386371.1:p.Lys65ArgfsTer?
NM_022336.3:c.192_198del (EDAR) NP_071731.1:p.Lys65ArgfsTer?
XM_006712204.1:c.192_198del (EDAR) XP_006712267.1:p.Lys65ArgfsTer?
XM_011510502.1:c.243_249del (EDAR) XP_011508804.1:p.Lys82ArgfsTer?
XM_011510503.1:c.243_249del (EDAR) XP_011508805.1:p.Lys82ArgfsTer?
XM_011510502.2:c.336_342del (EDAR) XP_011508804.2:p.Lys113ArgfsTer?
XM_011510503.2:c.336_342del (EDAR) XP_011508805.2:p.Lys113ArgfsTer?
XM_017004623.2:c.8370+156312_8370+156318del (RANBP2) XP_016860112.1:n.8370+156312_8370+156318d...
NM_022336.4:c.192_198del (EDAR) MANE Select NP_071731.1:p.Lys65ArgfsTer?