Canonical Allele Identifier: CA2677349922

Gene: EDN1

Linked Data

• gnomAD v4: 6-12292196-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12292196C>T , CM000668.2:g.12292196C>T	GRCh38
NC_000006.11:g.12292429C>T , CM000668.1:g.12292429C>T	GRCh37
NC_000006.10:g.12400415C>T	NCBI36
NG_016196.1:g.6901C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000379375.6:c.65-145C>T MANE Select	ENSP00000368683.5:n.65-145C>T
ENST00000379375.5:c.65-145C>T	ENSP00000368683.5:n.65-145C>T
NM_001168319.1:c.65-148C>T	NP_001161791.1:n.65-148C>T
NM_001955.4:c.65-145C>T	NP_001946.3:n.65-145C>T
XM_011514330.1:c.65-145C>T	XP_011512632.1:n.65-145C>T
XM_011514331.1:c.65-145C>T	XP_011512633.1:n.65-145C>T
XM_011514332.1:c.65-148C>T	XP_011512634.1:n.65-148C>T
XM_011514330.2:c.65-145C>T	XP_011512632.1:n.65-145C>T
XM_011514331.3:c.65-145C>T	XP_011512633.1:n.65-145C>T
XM_011514332.2:c.65-148C>T	XP_011512634.1:n.65-148C>T
XM_017010331.1:c.65-145C>T	XP_016865820.1:n.65-145C>T
NM_001955.5:c.65-145C>T MANE Select	NP_001946.3:n.65-145C>T
NM_001168319.2:c.65-148C>T	NP_001161791.1:n.65-148C>T