Canonical Allele Identifier: CA2435981900
Gene: EDA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70035378T= , CM000685.2:g.70035378T= GRCh38
NC_000023.10:g.69255228T= , CM000685.1:g.69255228T= GRCh37
NC_000023.9:g.69171953T= NCBI36
NG_009809.1:g.424318T=
NG_009809.2:g.424312T=

Transcript Alleles

HGVS Amino-acid change
ENST00000374552.9:c.945T= MANE Select ENSP00000363680.4:p.Thr315=
ENST00000374552.8:c.945T= ENSP00000363680.4:p.Thr315=
ENST00000374553.6:c.939T= ENSP00000363681.2:p.Thr313=
ENST00000524573.5:c.930T= ENSP00000432585.1:p.Thr310=
ENST00000616899.1:c.549T= ENSP00000481963.1:p.Thr183=
NM_001005609.1:c.939T= NP_001005609.1:p.Thr313=
NM_001005612.2:c.930T= NP_001005612.2:p.Thr310=
NM_001399.4:c.945T= NP_001390.1:p.Thr315=
XM_006724630.2:c.936T= XP_006724693.1:p.Thr312=
XM_017029336.1:c.903T= XP_016884825.1:p.Thr301=
NM_001399.5:c.945T= MANE Select NP_001390.1:p.Thr315=
NM_001005609.2:c.939T= NP_001005609.1:p.Thr313=
NM_001005612.3:c.930T= NP_001005612.2:p.Thr310=