Canonical Allele Identifier: CA1610829278

Gene: EDN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12294465T= , CM000668.2:g.12294465T=	GRCh38
NC_000006.11:g.12294698T= , CM000668.1:g.12294698T=	GRCh37
NC_000006.10:g.12402684T=	NCBI36
NG_016196.1:g.9170T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379375.6:c.533+61T= MANE Select	ENSP00000368683.5:n.533+61T=
ENST00000379375.5:c.533+61T=	ENSP00000368683.5:n.533+61T=
NM_001168319.1:c.530+61T=	NP_001161791.1:n.530+61T=
NM_001955.4:c.533+61T=	NP_001946.3:n.533+61T=
XM_011514330.1:c.533+61T=	XP_011512632.1:n.533+61T=
XM_011514331.1:c.533+61T=	XP_011512633.1:n.533+61T=
XM_011514332.1:c.530+61T=	XP_011512634.1:n.530+61T=
XM_011514330.2:c.533+61T=	XP_011512632.1:n.533+61T=
XM_011514331.3:c.533+61T=	XP_011512633.1:n.533+61T=
XM_011514332.2:c.530+61T=	XP_011512634.1:n.530+61T=
XM_017010331.1:c.533+61T=	XP_016865820.1:n.533+61T=
NM_001955.5:c.533+61T= MANE Select	NP_001946.3:n.533+61T=
NM_001168319.2:c.530+61T=	NP_001161791.1:n.530+61T=