Canonical Allele Identifier: CA413448188
Gene: EDA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70027863A>T , CM000685.2:g.70027863A>T GRCh38
NC_000023.10:g.69247713A>T , CM000685.1:g.69247713A>T GRCh37
NC_000023.9:g.69164438A>T NCBI36
NG_009809.1:g.416803A>T
NG_009809.2:g.416797A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000374552.9:c.533A>T MANE Select ENSP00000363680.4:p.Lys178Ile
ENST00000374552.8:c.533A>T ENSP00000363680.4:p.Lys178Ile
ENST00000374553.6:c.533A>T ENSP00000363681.2:p.Lys178Ile
ENST00000503592.5:c.137A>T ENSP00000423037.1:p.Lys46Ile
ENST00000524573.5:c.533A>T ENSP00000432585.1:p.Lys178Ile
ENST00000616899.1:c.137A>T ENSP00000481963.1:p.Lys46Ile
NM_001005609.1:c.533A>T NP_001005609.1:p.Lys178Ile
NM_001005612.2:c.533A>T NP_001005612.2:p.Lys178Ile
NM_001399.4:c.533A>T NP_001390.1:p.Lys178Ile
XM_006724630.2:c.533A>T XP_006724693.1:p.Lys178Ile
XM_011530885.1:c.533A>T XP_011529187.1:p.Lys178Ile
XM_011530885.2:c.533A>T XP_011529187.1:p.Lys178Ile
XM_017029336.1:c.533A>T XP_016884825.1:p.Lys178Ile
NM_001399.5:c.533A>T MANE Select NP_001390.1:p.Lys178Ile
NM_001005609.2:c.533A>T NP_001005609.1:p.Lys178Ile
NM_001005612.3:c.533A>T NP_001005612.2:p.Lys178Ile