Canonical Allele Identifier: CA1469996
Community Standard Title: NM_145861.4(EDARADD):c.161-33G>C
Gene: EDARADD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236427359G>C , CM000663.2:g.236427359G>C GRCh38
NC_000001.10:g.236590659G>C , CM000663.1:g.236590659G>C GRCh37
NC_000001.9:g.234657282G>C NCBI36
NG_011566.1:g.37980G>C

Transcript Alleles

HGVS Amino-acid Change
NM_145861.4:c.161-33G>C MANE Select NP_665860.2:n.161-33G>C
ENST00000334232.9:c.161-33G>C MANE Select ENSP00000335076.4:n.161-33G>C
NM_080738.3:c.131-33G>C NP_542776.1:n.131-33G>C
NM_080738.4:c.131-33G>C NP_542776.1:n.131-33G>C
NM_145861.2:c.161-33G>C NP_665860.2:n.161-33G>C
ENST00000334232.8:c.161-33G>C ENSP00000335076.4:n.161-33G>C
ENST00000359362.5:c.131-33G>C ENSP00000352320.4:n.131-33G>C
ENST00000359362.6:c.131-33G>C ENSP00000352320.4:n.131-33G>C
ENST00000439430.5:c.95-33G>C ENSP00000405815.1:n.95-33G>C
ENST00000637660.1:c.95-33G>C ENSP00000490347.1:n.95-33G>C
ENST00000642595.1:c.131-33G>C ENSP00000494458.1:n.131-33G>C