Canonical Allele Identifier: CA1610841619

Gene: EDN1

Linked Data

• dbSNP Id: rs1800997

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12290498_12290499del , CM000668.2:g.12290498_12290499del	GRCh38
NC_000006.11:g.12290731_12290732del , CM000668.1:g.12290731_12290732del	GRCh37
NC_000006.10:g.12398717_12398718del	NCBI36
NG_016196.1:g.5203_5204del

Transcript Alleles

HGVS	Amino-acid change
ENST00000379375.6:c.-132_-131del MANE Select	ENSP00000368683.5:n.-132_-131del
ENST00000379375.5:c.-132_-131del	ENSP00000368683.5:n.-132_-131del
NM_001168319.1:c.-132_-131del	NP_001161791.1:n.-132_-131del
NM_001955.4:c.-132_-131del	NP_001946.3:n.-132_-131del
XM_011514330.1:c.-1-131_-1-130del	XP_011512632.1:n.-1-131_-1-130del
XM_011514331.1:c.-1-131_-1-130del	XP_011512633.1:n.-1-131_-1-130del
XM_011514332.1:c.-1-131_-1-130del	XP_011512634.1:n.-1-131_-1-130del
XM_011514330.2:c.-1-131_-1-130del	XP_011512632.1:n.-1-131_-1-130del
XM_011514331.3:c.-1-131_-1-130del	XP_011512633.1:n.-1-131_-1-130del
XM_011514332.2:c.-1-131_-1-130del	XP_011512634.1:n.-1-131_-1-130del
XM_017010331.1:c.-1-131_-1-130del	XP_016865820.1:n.-1-131_-1-130del
NM_001955.5:c.-132_-131del MANE Select	NP_001946.3:n.-132_-131del
NM_001168319.2:c.-132_-131del	NP_001161791.1:n.-132_-131del