Canonical Allele Identifier: CA2695234461
Gene: EDA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70033502_70033536del , CM000685.2:g.70033502_70033536del GRCh38
NC_000023.10:g.69253352_69253386del , CM000685.1:g.69253352_69253386del GRCh37
NC_000023.9:g.69170077_69170111del NCBI36
NG_009809.1:g.422442_422476del
NG_009809.2:g.422436_422470del

Transcript Alleles

HGVS Amino-acid change
ENST00000374552.9:c.898_924+8del
ENST00000374552.8:c.898_924+8del
ENST00000374553.6:c.898_918+14del
ENST00000524573.5:c.889_909+14del
ENST00000616899.1:c.502_528+8del
NM_001005609.1:c.898_918+14del
NM_001005612.2:c.889_909+14del
NM_001399.4:c.898_924+8del
XM_006724630.2:c.889_915+8del
XM_011530885.1:c.898_918+14del
XM_011530885.2:c.898_918+14del
XM_017029336.1:c.882+16_882+50del XP_016884825.1:n.882+16_882+50del
NM_001399.5:c.898_924+8del
NM_001005609.2:c.898_918+14del
NM_001005612.3:c.889_909+14del