Canonical Allele Identifier: CA650509097

Gene: EDN1

Linked Data

• COSMIC: COSN21605962

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12290366_12290367insA , CM000668.2:g.12290366_12290367insA	GRCh38
NC_000006.11:g.12290599_12290600insA , CM000668.1:g.12290599_12290600insA	GRCh37
NC_000006.10:g.12398585_12398586insA	NCBI36
NG_016196.1:g.5071_5072insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379375.6:c.-264_-263insA MANE Select	ENSP00000368683.5:n.-264_-263insA
ENST00000379375.5:c.-264_-263insA	ENSP00000368683.5:n.-264_-263insA
NM_001168319.1:c.-264_-263insA	NP_001161791.1:n.-264_-263insA
NM_001955.4:c.-264_-263insA	NP_001946.3:n.-264_-263insA
XM_011514330.1:c.-1-263_-1-262insA	XP_011512632.1:n.-1-263_-1-262insA
XM_011514331.1:c.-1-263_-1-262insA	XP_011512633.1:n.-1-263_-1-262insA
XM_011514332.1:c.-1-263_-1-262insA	XP_011512634.1:n.-1-263_-1-262insA
XM_011514330.2:c.-1-263_-1-262insA	XP_011512632.1:n.-1-263_-1-262insA
XM_011514331.3:c.-1-263_-1-262insA	XP_011512633.1:n.-1-263_-1-262insA
XM_011514332.2:c.-1-263_-1-262insA	XP_011512634.1:n.-1-263_-1-262insA
XM_017010331.1:c.-2+243_-2+244insA	XP_016865820.1:n.-2+243_-2+244insA
NM_001955.5:c.-264_-263insA MANE Select	NP_001946.3:n.-264_-263insA
NM_001168319.2:c.-264_-263insA	NP_001161791.1:n.-264_-263insA