Canonical Allele Identifier: CA1610829172

Gene: EDN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12294386A= , CM000668.2:g.12294386A=	GRCh38
NC_000006.11:g.12294619A= , CM000668.1:g.12294619A=	GRCh37
NC_000006.10:g.12402605A=	NCBI36
NG_016196.1:g.9091A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379375.6:c.515A= MANE Select	ENSP00000368683.5:p.Glu172=
ENST00000379375.5:c.515A=	ENSP00000368683.5:p.Glu172=
NM_001168319.1:c.512A=	NP_001161791.1:p.Glu171=
NM_001955.4:c.515A=	NP_001946.3:p.Glu172=
XM_011514330.1:c.515A=	XP_011512632.1:p.Glu172=
XM_011514331.1:c.515A=	XP_011512633.1:p.Glu172=
XM_011514332.1:c.512A=	XP_011512634.1:p.Glu171=
XM_011514330.2:c.515A=	XP_011512632.1:p.Glu172=
XM_011514331.3:c.515A=	XP_011512633.1:p.Glu172=
XM_011514332.2:c.512A=	XP_011512634.1:p.Glu171=
XM_017010331.1:c.515A=	XP_016865820.1:p.Glu172=
NM_001955.5:c.515A= MANE Select	NP_001946.3:p.Glu172=
NM_001168319.2:c.512A=	NP_001161791.1:p.Glu171=