Canonical Allele Identifier: CA818251346
Gene: EDN1 HGNC NCBI

Linked Data

dbSNP Id: rs1395346493

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.12290424del , CM000668.2:g.12290424del GRCh38
NC_000006.11:g.12290657del , CM000668.1:g.12290657del GRCh37
NC_000006.10:g.12398643del NCBI36
NG_016196.1:g.5129del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379375.6:c.-206del MANE Select ENSP00000368683.5:n.-206del
ENST00000379375.5:c.-206del ENSP00000368683.5:n.-206del
NM_001168319.1:c.-206del NP_001161791.1:n.-206del
NM_001955.4:c.-206del NP_001946.3:n.-206del
XM_011514330.1:c.-1-205del XP_011512632.1:n.-1-205del
XM_011514331.1:c.-1-205del XP_011512633.1:n.-1-205del
XM_011514332.1:c.-1-205del XP_011512634.1:n.-1-205del
XM_011514330.2:c.-1-205del XP_011512632.1:n.-1-205del
XM_011514331.3:c.-1-205del XP_011512633.1:n.-1-205del
XM_011514332.2:c.-1-205del XP_011512634.1:n.-1-205del
XM_017010331.1:c.-1-205del XP_016865820.1:n.-1-205del
NM_001955.5:c.-206del MANE Select NP_001946.3:n.-206del
NM_001168319.2:c.-206del NP_001161791.1:n.-206del