Canonical Allele Identifier: CA2677349737

Gene: EDN1

Linked Data

• gnomAD v4: 6-12290488-TCCCCG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12290489_12290493del , CM000668.2:g.12290489_12290493del	GRCh38
NC_000006.11:g.12290722_12290726del , CM000668.1:g.12290722_12290726del	GRCh37
NC_000006.10:g.12398708_12398712del	NCBI36
NG_016196.1:g.5194_5198del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379375.6:c.-141_-137del MANE Select	ENSP00000368683.5:n.-141_-137del
ENST00000379375.5:c.-141_-137del	ENSP00000368683.5:n.-141_-137del
NM_001168319.1:c.-141_-137del	NP_001161791.1:n.-141_-137del
NM_001955.4:c.-141_-137del	NP_001946.3:n.-141_-137del
XM_011514330.1:c.-1-140_-1-136del	XP_011512632.1:n.-1-140_-1-136del
XM_011514331.1:c.-1-140_-1-136del	XP_011512633.1:n.-1-140_-1-136del
XM_011514332.1:c.-1-140_-1-136del	XP_011512634.1:n.-1-140_-1-136del
XM_011514330.2:c.-1-140_-1-136del	XP_011512632.1:n.-1-140_-1-136del
XM_011514331.3:c.-1-140_-1-136del	XP_011512633.1:n.-1-140_-1-136del
XM_011514332.2:c.-1-140_-1-136del	XP_011512634.1:n.-1-140_-1-136del
XM_017010331.1:c.-1-140_-1-136del	XP_016865820.1:n.-1-140_-1-136del
NM_001955.5:c.-141_-137del MANE Select	NP_001946.3:n.-141_-137del
NM_001168319.2:c.-141_-137del	NP_001161791.1:n.-141_-137del