Canonical Allele Identifier: CA1610841469
Gene: EDN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.12290421_12290424delinsTCCA , CM000668.2:g.12290421_12290424delinsTCCA GRCh38
NC_000006.11:g.12290654_12290657delinsTCCA , CM000668.1:g.12290654_12290657delinsTCCA GRCh37
NC_000006.10:g.12398640_12398643delinsTCCA NCBI36
NG_016196.1:g.5126_5129delinsTCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000379375.6:c.-209_-206delinsTCCA MANE Select ENSP00000368683.5:n.-209_-206delinsTCCA
ENST00000379375.5:c.-209_-206delinsTCCA ENSP00000368683.5:n.-209_-206delinsTCCA
NM_001168319.1:c.-209_-206delinsTCCA NP_001161791.1:n.-209_-206delinsTCCA
NM_001955.4:c.-209_-206delinsTCCA NP_001946.3:n.-209_-206delinsTCCA
XM_011514330.1:c.-1-208_-1-205delinsTCCA XP_011512632.1:n.-1-208_-1-205delinsTCCA
XM_011514331.1:c.-1-208_-1-205delinsTCCA XP_011512633.1:n.-1-208_-1-205delinsTCCA
XM_011514332.1:c.-1-208_-1-205delinsTCCA XP_011512634.1:n.-1-208_-1-205delinsTCCA
XM_011514330.2:c.-1-208_-1-205delinsTCCA XP_011512632.1:n.-1-208_-1-205delinsTCCA
XM_011514331.3:c.-1-208_-1-205delinsTCCA XP_011512633.1:n.-1-208_-1-205delinsTCCA
XM_011514332.2:c.-1-208_-1-205delinsTCCA XP_011512634.1:n.-1-208_-1-205delinsTCCA
XM_017010331.1:c.-1-208_-1-205delinsTCCA XP_016865820.1:n.-1-208_-1-205delinsTCCA
NM_001955.5:c.-209_-206delinsTCCA MANE Select NP_001946.3:n.-209_-206delinsTCCA
NM_001168319.2:c.-209_-206delinsTCCA NP_001161791.1:n.-209_-206delinsTCCA