Canonical Allele Identifier: CA917677453

Gene: EDN1

Linked Data

• dbSNP Id: rs10478721

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12293928_12293929dup , CM000668.2:g.12293928_12293929dup	GRCh38
NC_000006.11:g.12294161_12294162dup , CM000668.1:g.12294161_12294162dup	GRCh37
NC_000006.10:g.12402147_12402148dup	NCBI36
NG_016196.1:g.8633_8634dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379375.6:c.234-13_234-12dup MANE Select	ENSP00000368683.5:n.234-13_234-12dup
ENST00000379375.5:c.234-13_234-12dup	ENSP00000368683.5:n.234-13_234-12dup
NM_001168319.1:c.231-13_231-12dup	NP_001161791.1:n.231-13_231-12dup
NM_001955.4:c.234-13_234-12dup	NP_001946.3:n.234-13_234-12dup
XM_011514330.1:c.234-13_234-12dup	XP_011512632.1:n.234-13_234-12dup
XM_011514331.1:c.234-13_234-12dup	XP_011512633.1:n.234-13_234-12dup
XM_011514332.1:c.231-13_231-12dup	XP_011512634.1:n.231-13_231-12dup
XM_011514330.2:c.234-13_234-12dup	XP_011512632.1:n.234-13_234-12dup
XM_011514331.3:c.234-13_234-12dup	XP_011512633.1:n.234-13_234-12dup
XM_011514332.2:c.231-13_231-12dup	XP_011512634.1:n.231-13_231-12dup
XM_017010331.1:c.234-13_234-12dup	XP_016865820.1:n.234-13_234-12dup
NM_001955.5:c.234-13_234-12dup MANE Select	NP_001946.3:n.234-13_234-12dup
NM_001168319.2:c.231-13_231-12dup	NP_001161791.1:n.231-13_231-12dup