Canonical Allele Identifier: CA150779

Gene: EDN1

Linked Data

• ClinVar Variation Id: 120212
• ClinVar RCV Id: RCV000106312
• dbSNP Id: rs587777231
• MyVariant Identifiers: chr6:g.12294211A>G (hg19) ; chr6:g.12293978A>G (hg38)
• PubMed: PMID:23315542 ; PMID:24268655

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12293978A>G , CM000668.2:g.12293978A>G	GRCh38
NC_000006.11:g.12294211A>G , CM000668.1:g.12294211A>G	GRCh37
NC_000006.10:g.12402197A>G	NCBI36
NG_016196.1:g.8683A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379375.6:c.271A>G MANE Select	ENSP00000368683.5:p.Lys91Glu
ENST00000379375.5:c.271A>G	ENSP00000368683.5:p.Lys91Glu
NM_001168319.1:c.268A>G	NP_001161791.1:p.Lys90Glu
NM_001955.4:c.271A>G	NP_001946.3:p.Lys91Glu
XM_011514330.1:c.271A>G	XP_011512632.1:p.Lys91Glu
XM_011514331.1:c.271A>G	XP_011512633.1:p.Lys91Glu
XM_011514332.1:c.268A>G	XP_011512634.1:p.Lys90Glu
XM_011514330.2:c.271A>G	XP_011512632.1:p.Lys91Glu
XM_011514331.3:c.271A>G	XP_011512633.1:p.Lys91Glu
XM_011514332.2:c.268A>G	XP_011512634.1:p.Lys90Glu
XM_017010331.1:c.271A>G	XP_016865820.1:p.Lys91Glu
NM_001955.5:c.271A>G MANE Select	NP_001946.3:p.Lys91Glu
NM_001168319.2:c.268A>G	NP_001161791.1:p.Lys90Glu