Canonical Allele Identifier: CA657711898
Gene: EDA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.69616300_69616301insT , CM000685.2:g.69616300_69616301insT GRCh38
NC_000023.10:g.68836144_68836145insT , CM000685.1:g.68836144_68836145insT GRCh37
NC_000023.9:g.68752869_68752870insT NCBI36
NG_009809.1:g.5234_5235insT
NG_009809.2:g.5234_5235insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000374552.9:c.-9_-8insT MANE Select ENSP00000363680.4:n.-9_-8insT
ENST00000338901.4:c.-9_-8insT ENSP00000340611.4:n.-9_-8insT
ENST00000374548.5:n.234_235insT
ENST00000374552.8:c.-9_-8insT ENSP00000363680.4:n.-9_-8insT
ENST00000374553.6:c.-9_-8insT ENSP00000363681.2:n.-9_-8insT
ENST00000502251.5:n.234_235insT
ENST00000524573.5:c.-9_-8insT ENSP00000432585.1:n.-9_-8insT
ENST00000525810.5:c.-9_-8insT ENSP00000434195.1:n.-9_-8insT
ENST00000527388.5:c.-9_-8insT ENSP00000434861.1:n.-9_-8insT
ENST00000533317.5:n.234_235insT
NM_001005609.1:c.-9_-8insT NP_001005609.1:n.-9_-8insT
NM_001005610.3:c.-9_-8insT NP_001005610.2:n.-9_-8insT
NM_001005612.2:c.-9_-8insT NP_001005612.2:n.-9_-8insT
NM_001005613.3:c.-9_-8insT NP_001005613.1:n.-9_-8insT
NM_001399.4:c.-9_-8insT NP_001390.1:n.-9_-8insT
XM_006724630.2:c.-9_-8insT XP_006724693.1:n.-9_-8insT
XM_011530885.1:c.-9_-8insT XP_011529187.1:n.-9_-8insT
XM_011530885.2:c.-9_-8insT XP_011529187.1:n.-9_-8insT
XM_017029336.1:c.-9_-8insT XP_016884825.1:n.-9_-8insT
XM_017029337.1:c.-9_-8insT XP_016884826.1:n.-9_-8insT
XR_001755660.1:n.215_216insT
NM_001399.5:c.-9_-8insT MANE Select NP_001390.1:n.-9_-8insT
NM_001005609.2:c.-9_-8insT NP_001005609.1:n.-9_-8insT
NM_001005610.4:c.-9_-8insT NP_001005610.2:n.-9_-8insT
NM_001005612.3:c.-9_-8insT NP_001005612.2:n.-9_-8insT
NM_001005613.4:c.-9_-8insT NP_001005613.1:n.-9_-8insT