Canonical Allele Identifier: CA1610840985
Gene: EDN1 HGNC NCBI

Linked Data

dbSNP Id: rs1762636902

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.12290276_12290279del , CM000668.2:g.12290276_12290279del GRCh38
NC_000006.11:g.12290509_12290512del , CM000668.1:g.12290509_12290512del GRCh37
NC_000006.10:g.12398495_12398498del NCBI36
NG_016196.1:g.4981_4984del

Transcript Alleles

HGVS Amino-acid Change
XM_011514330.1:c.-1-353_-1-350del XP_011512632.1:n.-1-353_-1-350del
XM_011514331.1:c.-1-353_-1-350del XP_011512633.1:n.-1-353_-1-350del
XM_011514332.1:c.-1-353_-1-350del XP_011512634.1:n.-1-353_-1-350del
XM_011514330.2:c.-1-353_-1-350del XP_011512632.1:n.-1-353_-1-350del
XM_011514331.3:c.-1-353_-1-350del XP_011512633.1:n.-1-353_-1-350del
XM_011514332.2:c.-1-353_-1-350del XP_011512634.1:n.-1-353_-1-350del
XM_017010331.1:c.-2+153_-2+156del XP_016865820.1:n.-2+153_-2+156del