Canonical Allele Identifier: CA2581541179

Gene: EDN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12293904T>A , CM000668.2:g.12293904T>A	GRCh38
NC_000006.11:g.12294137T>A , CM000668.1:g.12294137T>A	GRCh37
NC_000006.10:g.12402123T>A	NCBI36
NG_016196.1:g.8609T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000379375.6:c.234-37T>A MANE Select	ENSP00000368683.5:n.234-37T>A
ENST00000379375.5:c.234-37T>A	ENSP00000368683.5:n.234-37T>A
NM_001168319.1:c.231-37T>A	NP_001161791.1:n.231-37T>A
NM_001955.4:c.234-37T>A	NP_001946.3:n.234-37T>A
XM_011514330.1:c.234-37T>A	XP_011512632.1:n.234-37T>A
XM_011514331.1:c.234-37T>A	XP_011512633.1:n.234-37T>A
XM_011514332.1:c.231-37T>A	XP_011512634.1:n.231-37T>A
XM_011514330.2:c.234-37T>A	XP_011512632.1:n.234-37T>A
XM_011514331.3:c.234-37T>A	XP_011512633.1:n.234-37T>A
XM_011514332.2:c.231-37T>A	XP_011512634.1:n.231-37T>A
XM_017010331.1:c.234-37T>A	XP_016865820.1:n.234-37T>A
NM_001955.5:c.234-37T>A MANE Select	NP_001946.3:n.234-37T>A
NM_001168319.2:c.231-37T>A	NP_001161791.1:n.231-37T>A