Canonical Allele Identifier: CA413447568
Gene: EDA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.69616647G>T , CM000685.2:g.69616647G>T GRCh38
NC_000023.10:g.68836491G>T , CM000685.1:g.68836491G>T GRCh37
NC_000023.9:g.68753216G>T NCBI36
NG_009809.1:g.5581G>T
NG_009809.2:g.5581G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374552.9:c.339G>T MANE Select ENSP00000363680.4:p.Gln113His
ENST00000338901.4:c.339G>T ENSP00000340611.4:p.Gln113His
ENST00000374548.5:n.581G>T
ENST00000374552.8:c.339G>T ENSP00000363680.4:p.Gln113His
ENST00000374553.6:c.339G>T ENSP00000363681.2:p.Gln113His
ENST00000502251.5:n.581G>T
ENST00000524573.5:c.339G>T ENSP00000432585.1:p.Gln113His
ENST00000525810.5:c.339G>T ENSP00000434195.1:p.Gln113His
ENST00000527388.5:c.339G>T ENSP00000434861.1:p.Gln113His
ENST00000533317.5:n.581G>T
NM_001005609.1:c.339G>T NP_001005609.1:p.Gln113His
NM_001005610.3:c.339G>T NP_001005610.2:p.Gln113His
NM_001005612.2:c.339G>T NP_001005612.2:p.Gln113His
NM_001005613.3:c.339G>T NP_001005613.1:p.Gln113His
NM_001399.4:c.339G>T NP_001390.1:p.Gln113His
XM_006724630.2:c.339G>T XP_006724693.1:p.Gln113His
XM_011530885.1:c.339G>T XP_011529187.1:p.Gln113His
XM_011530885.2:c.339G>T XP_011529187.1:p.Gln113His
XM_017029336.1:c.339G>T XP_016884825.1:p.Gln113His
XM_017029337.1:c.339G>T XP_016884826.1:p.Gln113His
XR_001755660.1:n.562G>T
NM_001399.5:c.339G>T MANE Select NP_001390.1:p.Gln113His
NM_001005609.2:c.339G>T NP_001005609.1:p.Gln113His
NM_001005610.4:c.339G>T NP_001005610.2:p.Gln113His
NM_001005612.3:c.339G>T NP_001005612.2:p.Gln113His
NM_001005613.4:c.339G>T NP_001005613.1:p.Gln113His