Canonical Allele Identifier: CA2770023603
Gene: EDN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.12290438_12290439insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAGGTCGGGCAGGCGGCGGGCACGCACCACGAACTTACGGATATTGATGCTCGTGTGCCTGCGAGTAATATCCGGAATCACCGCG , CM000668.2:g.12290438_12290439insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAGGTCGGGCAGGCGGCGGGCACGCACCACGAACTTACGGATATTGATGCTCGTGTGCCTGCGAGTAATATCCGGAATCACCGCG GRCh38
NC_000006.11:g.12290671_12290672insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAGGTCGGGCAGGCGGCGGGCACGCACCACGAACTTACGGATATTGATGCTCGTGTGCCTGCGAGTAATATCCGGAATCACCGCG , CM000668.1:g.12290671_12290672insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAGGTCGGGCAGGCGGCGGGCACGCACCACGAACTTACGGATATTGATGCTCGTGTGCCTGCGAGTAATATCCGGAATCACCGCG GRCh37
NC_000006.10:g.12398657_12398658insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAGGTCGGGCAGGCGGCGGGCACGCACCACGAACTTACGGATATTGATGCTCGTGTGCCTGCGAGTAATATCCGGAATCACCGCG NCBI36
NG_016196.1:g.5143_5144insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAGGTCGGGCAGGCGGCGGGCACGCACCACGAACTTACGGATATTGATGCTCGTGTGCCTGCGAGTAATATCCGGAATCACCGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000379375.6:c.-192_-191insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAGGTCGGGCAGGCGGCGGGCACGCACCACGAACTTACGGATATTGATGCTCGTGTGCCTGCGAGTAATATCCGGAATCACCGCG MANE Select ENSP00000368683.5:n.-192_-191insGCGCCGGCGCTCAGCGAGTTCATGCGCAC...
ENST00000379375.5:c.-192_-191insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAGGTCGGGCAGGCGGCGGGCACGCACCACGAACTTACGGATATTGATGCTCGTGTGCCTGCGAGTAATATCCGGAATCACCGCG ENSP00000368683.5:n.-192_-191insGCGCCGGCGCTCAGCGAGTTCATGCGCAC...
NM_001168319.1:c.-192_-191insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAGGTCGGGCAGGCGGCGGGCACGCACCACGAACTTACGGATATTGATGCTCGTGTGCCTGCGAGTAATATCCGGAATCACCGCG NP_001161791.1:n.-192_-191insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAG...
NM_001955.4:c.-192_-191insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAGGTCGGGCAGGCGGCGGGCACGCACCACGAACTTACGGATATTGATGCTCGTGTGCCTGCGAGTAATATCCGGAATCACCGCG NP_001946.3:n.-192_-191insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAGGTC...
XM_011514330.1:c.-1-191_-1-190insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAGGTCGGGCAGGCGGCGGGCACGCACCACGAACTTACGGATATTGATGCTCGTGTGCCTGCGAGTAATATCCGGAATCACCGCG XP_011512632.1:n.-1-191_-1-190insGCGCCGGCGCTCAGCGAGTTCATGCGCA...
XM_011514331.1:c.-1-191_-1-190insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAGGTCGGGCAGGCGGCGGGCACGCACCACGAACTTACGGATATTGATGCTCGTGTGCCTGCGAGTAATATCCGGAATCACCGCG XP_011512633.1:n.-1-191_-1-190insGCGCCGGCGCTCAGCGAGTTCATGCGCA...
XM_011514332.1:c.-1-191_-1-190insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAGGTCGGGCAGGCGGCGGGCACGCACCACGAACTTACGGATATTGATGCTCGTGTGCCTGCGAGTAATATCCGGAATCACCGCG XP_011512634.1:n.-1-191_-1-190insGCGCCGGCGCTCAGCGAGTTCATGCGCA...
XM_011514330.2:c.-1-191_-1-190insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAGGTCGGGCAGGCGGCGGGCACGCACCACGAACTTACGGATATTGATGCTCGTGTGCCTGCGAGTAATATCCGGAATCACCGCG XP_011512632.1:n.-1-191_-1-190insGCGCCGGCGCTCAGCGAGTTCATGCGCA...
XM_011514331.3:c.-1-191_-1-190insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAGGTCGGGCAGGCGGCGGGCACGCACCACGAACTTACGGATATTGATGCTCGTGTGCCTGCGAGTAATATCCGGAATCACCGCG XP_011512633.1:n.-1-191_-1-190insGCGCCGGCGCTCAGCGAGTTCATGCGCA...
XM_011514332.2:c.-1-191_-1-190insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAGGTCGGGCAGGCGGCGGGCACGCACCACGAACTTACGGATATTGATGCTCGTGTGCCTGCGAGTAATATCCGGAATCACCGCG XP_011512634.1:n.-1-191_-1-190insGCGCCGGCGCTCAGCGAGTTCATGCGCA...
XM_017010331.1:c.-1-191_-1-190insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAGGTCGGGCAGGCGGCGGGCACGCACCACGAACTTACGGATATTGATGCTCGTGTGCCTGCGAGTAATATCCGGAATCACCGCG XP_016865820.1:n.-1-191_-1-190insGCGCCGGCGCTCAGCGAGTTCATGCGCA...
NM_001955.5:c.-192_-191insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAGGTCGGGCAGGCGGCGGGCACGCACCACGAACTTACGGATATTGATGCTCGTGTGCCTGCGAGTAATATCCGGAATCACCGCG MANE Select NP_001946.3:n.-192_-191insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAGGTC...
NM_001168319.2:c.-192_-191insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAGGTCGGGCAGGCGGCGGGCACGCACCACGAACTTACGGATATTGATGCTCGTGTGCCTGCGAGTAATATCCGGAATCACCGCG NP_001161791.1:n.-192_-191insGCGCCGGCGCTCAGCGAGTTCATGCGCACAAG...