Canonical Allele Identifier: CA2435981324
Gene: EDA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70033507C= , CM000685.2:g.70033507C= GRCh38
NC_000023.10:g.69253357C= , CM000685.1:g.69253357C= GRCh37
NC_000023.9:g.69170082C= NCBI36
NG_009809.1:g.422447C=
NG_009809.2:g.422441C=

Transcript Alleles

HGVS Amino-acid change
ENST00000374552.9:c.903C= MANE Select ENSP00000363680.4:p.Tyr301=
ENST00000374552.8:c.903C= ENSP00000363680.4:p.Tyr301=
ENST00000374553.6:c.903C= ENSP00000363681.2:p.Tyr301=
ENST00000524573.5:c.894C= ENSP00000432585.1:p.Tyr298=
ENST00000616899.1:c.507C= ENSP00000481963.1:p.Tyr169=
NM_001005609.1:c.903C= NP_001005609.1:p.Tyr301=
NM_001005612.2:c.894C= NP_001005612.2:p.Tyr298=
NM_001399.4:c.903C= NP_001390.1:p.Tyr301=
XM_006724630.2:c.894C= XP_006724693.1:p.Tyr298=
XM_011530885.1:c.903C= XP_011529187.1:p.Tyr301=
XM_011530885.2:c.903C= XP_011529187.1:p.Tyr301=
XM_017029336.1:c.882+21C= XP_016884825.1:n.882+21C=
NM_001399.5:c.903C= MANE Select NP_001390.1:p.Tyr301=
NM_001005609.2:c.903C= NP_001005609.1:p.Tyr301=
NM_001005612.3:c.894C= NP_001005612.2:p.Tyr298=