Canonical Allele Identifier: CA2693980075
Gene: EDA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70033326_70033328del , CM000685.2:g.70033326_70033328del GRCh38
NC_000023.10:g.69253176_69253178del , CM000685.1:g.69253176_69253178del GRCh37
NC_000023.9:g.69169901_69169903del NCBI36
NG_009809.1:g.422266_422268del
NG_009809.2:g.422260_422262del

Transcript Alleles

HGVS Amino-acid change
ENST00000374552.9:c.794-72_794-70del MANE Select ENSP00000363680.4:n.794-72_794-70del
ENST00000374552.8:c.794-72_794-70del ENSP00000363680.4:n.794-72_794-70del
ENST00000374553.6:c.794-72_794-70del ENSP00000363681.2:n.794-72_794-70del
ENST00000503592.5:c.398-72_398-70del ENSP00000423037.1:n.398-72_398-70del
ENST00000524573.5:c.794-81_794-79del ENSP00000432585.1:n.794-81_794-79del
ENST00000616899.1:c.398-72_398-70del ENSP00000481963.1:n.398-72_398-70del
NM_001005609.1:c.794-72_794-70del NP_001005609.1:n.794-72_794-70del
NM_001005612.2:c.794-81_794-79del NP_001005612.2:n.794-81_794-79del
NM_001399.4:c.794-72_794-70del NP_001390.1:n.794-72_794-70del
XM_006724630.2:c.794-81_794-79del XP_006724693.1:n.794-81_794-79del
XM_011530885.1:c.794-72_794-70del XP_011529187.1:n.794-72_794-70del
XM_011530885.2:c.794-72_794-70del XP_011529187.1:n.794-72_794-70del
XM_017029336.1:c.794-72_794-70del XP_016884825.1:n.794-72_794-70del
NM_001399.5:c.794-72_794-70del MANE Select NP_001390.1:n.794-72_794-70del
NM_001005609.2:c.794-72_794-70del NP_001005609.1:n.794-72_794-70del
NM_001005612.3:c.794-81_794-79del NP_001005612.2:n.794-81_794-79del