Canonical Allele Identifier: CA1610829153
Gene: EDN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.12294370A= , CM000668.2:g.12294370A= GRCh38
NC_000006.11:g.12294603A= , CM000668.1:g.12294603A= GRCh37
NC_000006.10:g.12402589A= NCBI36
NG_016196.1:g.9075A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379375.6:c.499A= MANE Select ENSP00000368683.5:p.Arg167=
ENST00000379375.5:c.499A= ENSP00000368683.5:p.Arg167=
NM_001168319.1:c.496A= NP_001161791.1:p.Arg166=
NM_001955.4:c.499A= NP_001946.3:p.Arg167=
XM_011514330.1:c.499A= XP_011512632.1:p.Arg167=
XM_011514331.1:c.499A= XP_011512633.1:p.Arg167=
XM_011514332.1:c.496A= XP_011512634.1:p.Arg166=
XM_011514330.2:c.499A= XP_011512632.1:p.Arg167=
XM_011514331.3:c.499A= XP_011512633.1:p.Arg167=
XM_011514332.2:c.496A= XP_011512634.1:p.Arg166=
XM_017010331.1:c.499A= XP_016865820.1:p.Arg167=
NM_001955.5:c.499A= MANE Select NP_001946.3:p.Arg167=
NM_001168319.2:c.496A= NP_001161791.1:p.Arg166=