Canonical Allele Identifier: CA2435981896
Gene: EDA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70035367A= , CM000685.2:g.70035367A= GRCh38
NC_000023.10:g.69255217A= , CM000685.1:g.69255217A= GRCh37
NC_000023.9:g.69171942A= NCBI36
NG_009809.1:g.424307A=
NG_009809.2:g.424301A=

Transcript Alleles

HGVS Amino-acid change
ENST00000374552.9:c.934A= MANE Select ENSP00000363680.4:p.Ile312=
ENST00000374552.8:c.934A= ENSP00000363680.4:p.Ile312=
ENST00000374553.6:c.928A= ENSP00000363681.2:p.Ile310=
ENST00000524573.5:c.919A= ENSP00000432585.1:p.Ile307=
ENST00000616899.1:c.538A= ENSP00000481963.1:p.Ile180=
NM_001005609.1:c.928A= NP_001005609.1:p.Ile310=
NM_001005612.2:c.919A= NP_001005612.2:p.Ile307=
NM_001399.4:c.934A= NP_001390.1:p.Ile312=
XM_006724630.2:c.925A= XP_006724693.1:p.Ile309=
XM_017029336.1:c.892A= XP_016884825.1:p.Ile298=
NM_001399.5:c.934A= MANE Select NP_001390.1:p.Ile312=
NM_001005609.2:c.928A= NP_001005609.1:p.Ile310=
NM_001005612.3:c.919A= NP_001005612.2:p.Ile307=