Canonical Allele Identifier: CA2435979588
Gene: EDA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70027964A= , CM000685.2:g.70027964A= GRCh38
NC_000023.10:g.69247814A= , CM000685.1:g.69247814A= GRCh37
NC_000023.9:g.69164539A= NCBI36
NG_009809.1:g.416904A=
NG_009809.2:g.416898A=

Transcript Alleles

HGVS Amino-acid change
ENST00000374552.9:c.634A= MANE Select ENSP00000363680.4:p.Thr212=
ENST00000374552.8:c.634A= ENSP00000363680.4:p.Thr212=
ENST00000374553.6:c.634A= ENSP00000363681.2:p.Thr212=
ENST00000503592.5:c.238A= ENSP00000423037.1:p.Thr80=
ENST00000524573.5:c.634A= ENSP00000432585.1:p.Thr212=
ENST00000616899.1:c.238A= ENSP00000481963.1:p.Thr80=
NM_001005609.1:c.634A= NP_001005609.1:p.Thr212=
NM_001005612.2:c.634A= NP_001005612.2:p.Thr212=
NM_001399.4:c.634A= NP_001390.1:p.Thr212=
XM_006724630.2:c.634A= XP_006724693.1:p.Thr212=
XM_011530885.1:c.634A= XP_011529187.1:p.Thr212=
XM_011530885.2:c.634A= XP_011529187.1:p.Thr212=
XM_017029336.1:c.634A= XP_016884825.1:p.Thr212=
NM_001399.5:c.634A= MANE Select NP_001390.1:p.Thr212=
NM_001005609.2:c.634A= NP_001005609.1:p.Thr212=
NM_001005612.3:c.634A= NP_001005612.2:p.Thr212=