Canonical Allele Identifier: CA345353891
Gene: EDARADD HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.236645716T>A (hg19) chr1:g.236482416T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236482416T>A , CM000663.2:g.236482416T>A GRCh38
NC_000001.10:g.236645716T>A , CM000663.1:g.236645716T>A GRCh37
NC_000001.9:g.234712339T>A NCBI36
NG_011566.1:g.93037T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000334232.9:c.415T>A MANE Select ENSP00000335076.4:p.Trp139Arg
ENST00000359362.6:c.385T>A ENSP00000352320.4:p.Trp129Arg
ENST00000637660.1:c.349T>A ENSP00000490347.1:p.Trp117Arg
ENST00000642595.1:c.236-9321T>A ENSP00000494458.1:n.236-9321T>A
ENST00000334232.8:c.415T>A ENSP00000335076.4:p.Trp139Arg
ENST00000359362.5:c.385T>A ENSP00000352320.4:p.Trp129Arg
NM_080738.3:c.385T>A NP_542776.1:p.Trp129Arg
NM_145861.2:c.415T>A NP_665860.2:p.Trp139Arg
NM_080738.4:c.385T>A NP_542776.1:p.Trp129Arg
NM_145861.4:c.415T>A MANE Select NP_665860.2:p.Trp139Arg
Search 100 bp 5'
Search 100 bp 3'