Canonical Allele Identifier: CA1610841463

Gene: EDN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12290417G= , CM000668.2:g.12290417G=	GRCh38
NC_000006.11:g.12290650G= , CM000668.1:g.12290650G=	GRCh37
NC_000006.10:g.12398636G=	NCBI36
NG_016196.1:g.5122G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000379375.6:c.-213G= MANE Select	ENSP00000368683.5:n.-213G=
ENST00000379375.5:c.-213G=	ENSP00000368683.5:n.-213G=
NM_001168319.1:c.-213G=	NP_001161791.1:n.-213G=
NM_001955.4:c.-213G=	NP_001946.3:n.-213G=
XM_011514330.1:c.-1-212G=	XP_011512632.1:n.-1-212G=
XM_011514331.1:c.-1-212G=	XP_011512633.1:n.-1-212G=
XM_011514332.1:c.-1-212G=	XP_011512634.1:n.-1-212G=
XM_011514330.2:c.-1-212G=	XP_011512632.1:n.-1-212G=
XM_011514331.3:c.-1-212G=	XP_011512633.1:n.-1-212G=
XM_011514332.2:c.-1-212G=	XP_011512634.1:n.-1-212G=
XM_017010331.1:c.-1-212G=	XP_016865820.1:n.-1-212G=
NM_001955.5:c.-213G= MANE Select	NP_001946.3:n.-213G=
NM_001168319.2:c.-213G=	NP_001161791.1:n.-213G=