Canonical Allele Identifier: CA1610830735
Gene: EDN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.12295886T= , CM000668.2:g.12295886T= GRCh38
NC_000006.11:g.12296119T= , CM000668.1:g.12296119T= GRCh37
NC_000006.10:g.12404105T= NCBI36
NG_016196.1:g.10591T=

Transcript Alleles

HGVS Amino-acid change
ENST00000379375.6:c.534-76T= MANE Select ENSP00000368683.5:n.534-76T=
ENST00000379375.5:c.534-76T= ENSP00000368683.5:n.534-76T=
NM_001168319.1:c.531-76T= NP_001161791.1:n.531-76T=
NM_001955.4:c.534-76T= NP_001946.3:n.534-76T=
XM_011514330.1:c.534-76T= XP_011512632.1:n.534-76T=
XM_011514331.1:c.534-76T= XP_011512633.1:n.534-76T=
XM_011514332.1:c.531-76T= XP_011512634.1:n.531-76T=
XM_011514330.2:c.534-76T= XP_011512632.1:n.534-76T=
XM_011514331.3:c.534-76T= XP_011512633.1:n.534-76T=
XM_011514332.2:c.531-76T= XP_011512634.1:n.531-76T=
XM_017010331.1:c.534-76T= XP_016865820.1:n.534-76T=
NM_001955.5:c.534-76T= MANE Select NP_001946.3:n.534-76T=
NM_001168319.2:c.531-76T= NP_001161791.1:n.531-76T=