Canonical Allele Identifier: CA448427932
Gene: EDN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.12295962G>A , CM000668.2:g.12295962G>A GRCh38
NC_000006.11:g.12296195G>A , CM000668.1:g.12296195G>A GRCh37
NC_000006.10:g.12404181G>A NCBI36
NG_016196.1:g.10667G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379375.6:c.534G>A MANE Select ENSP00000368683.5:p.Arg178=
ENST00000379375.5:c.534G>A ENSP00000368683.5:p.Arg178=
NM_001168319.1:c.531G>A NP_001161791.1:p.Arg177=
NM_001955.4:c.534G>A NP_001946.3:p.Arg178=
XM_011514330.1:c.534G>A XP_011512632.1:p.Arg178=
XM_011514331.1:c.534G>A XP_011512633.1:p.Arg178=
XM_011514332.1:c.531G>A XP_011512634.1:p.Arg177=
XM_011514330.2:c.534G>A XP_011512632.1:p.Arg178=
XM_011514331.3:c.534G>A XP_011512633.1:p.Arg178=
XM_011514332.2:c.531G>A XP_011512634.1:p.Arg177=
XM_017010331.1:c.534G>A XP_016865820.1:p.Arg178=
NM_001955.5:c.534G>A MANE Select NP_001946.3:p.Arg178=
NM_001168319.2:c.531G>A NP_001161791.1:p.Arg177=