Canonical Allele Identifier: CA1610830984
Gene: EDN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.12296038T= , CM000668.2:g.12296038T= GRCh38
NC_000006.11:g.12296271T= , CM000668.1:g.12296271T= GRCh37
NC_000006.10:g.12404257T= NCBI36
NG_016196.1:g.10743T=

Transcript Alleles

HGVS Amino-acid change
ENST00000379375.6:c.610T= MANE Select ENSP00000368683.5:p.Tyr204=
ENST00000379375.5:c.610T= ENSP00000368683.5:p.Tyr204=
NM_001168319.1:c.607T= NP_001161791.1:p.Tyr203=
NM_001955.4:c.610T= NP_001946.3:p.Tyr204=
XM_011514330.1:c.610T= XP_011512632.1:p.Tyr204=
XM_011514331.1:c.610T= XP_011512633.1:p.Tyr204=
XM_011514332.1:c.607T= XP_011512634.1:p.Tyr203=
XM_011514330.2:c.610T= XP_011512632.1:p.Tyr204=
XM_011514331.3:c.610T= XP_011512633.1:p.Tyr204=
XM_011514332.2:c.607T= XP_011512634.1:p.Tyr203=
XM_017010331.1:c.610T= XP_016865820.1:p.Tyr204=
NM_001955.5:c.610T= MANE Select NP_001946.3:p.Tyr204=
NM_001168319.2:c.607T= NP_001161791.1:p.Tyr203=