Canonical Allele Identifier: CA1610841470

Gene: EDN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12290423_12290424delinsCA , CM000668.2:g.12290423_12290424delinsCA	GRCh38
NC_000006.11:g.12290656_12290657delinsCA , CM000668.1:g.12290656_12290657delinsCA	GRCh37
NC_000006.10:g.12398642_12398643delinsCA	NCBI36
NG_016196.1:g.5128_5129delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379375.6:c.-207_-206delinsCA MANE Select	ENSP00000368683.5:n.-207_-206delinsCA
ENST00000379375.5:c.-207_-206delinsCA	ENSP00000368683.5:n.-207_-206delinsCA
NM_001168319.1:c.-207_-206delinsCA	NP_001161791.1:n.-207_-206delinsCA
NM_001955.4:c.-207_-206delinsCA	NP_001946.3:n.-207_-206delinsCA
XM_011514330.1:c.-1-206_-1-205delinsCA	XP_011512632.1:n.-1-206_-1-205delinsCA
XM_011514331.1:c.-1-206_-1-205delinsCA	XP_011512633.1:n.-1-206_-1-205delinsCA
XM_011514332.1:c.-1-206_-1-205delinsCA	XP_011512634.1:n.-1-206_-1-205delinsCA
XM_011514330.2:c.-1-206_-1-205delinsCA	XP_011512632.1:n.-1-206_-1-205delinsCA
XM_011514331.3:c.-1-206_-1-205delinsCA	XP_011512633.1:n.-1-206_-1-205delinsCA
XM_011514332.2:c.-1-206_-1-205delinsCA	XP_011512634.1:n.-1-206_-1-205delinsCA
XM_017010331.1:c.-1-206_-1-205delinsCA	XP_016865820.1:n.-1-206_-1-205delinsCA
NM_001955.5:c.-207_-206delinsCA MANE Select	NP_001946.3:n.-207_-206delinsCA
NM_001168319.2:c.-207_-206delinsCA	NP_001161791.1:n.-207_-206delinsCA