Canonical Allele Identifier: CA2677350618

Gene: EDN1

Linked Data

• gnomAD v4: 6-12296481-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12296481A>G , CM000668.2:g.12296481A>G	GRCh38
NC_000006.11:g.12296714A>G , CM000668.1:g.12296714A>G	GRCh37
NC_000006.10:g.12404700A>G	NCBI36
NG_016196.1:g.11186A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379375.6:c.*414A>G MANE Select	ENSP00000368683.5:n.*414A>G
ENST00000379375.5:c.*414A>G	ENSP00000368683.5:n.*414A>G
NM_001168319.1:c.*414A>G	NP_001161791.1:n.*414A>G
NM_001955.4:c.*414A>G	NP_001946.3:n.*414A>G
XM_011514330.1:c.*414A>G	XP_011512632.1:n.*414A>G
XM_011514331.1:c.*414A>G	XP_011512633.1:n.*414A>G
XM_011514332.1:c.*414A>G	XP_011512634.1:n.*414A>G
XM_011514330.2:c.*414A>G	XP_011512632.1:n.*414A>G
XM_011514331.3:c.*414A>G	XP_011512633.1:n.*414A>G
XM_011514332.2:c.*414A>G	XP_011512634.1:n.*414A>G
XM_017010331.1:c.*414A>G	XP_016865820.1:n.*414A>G
NM_001955.5:c.*414A>G MANE Select	NP_001946.3:n.*414A>G
NM_001168319.2:c.*414A>G	NP_001161791.1:n.*414A>G