Canonical Allele Identifier: CA1610843566

Gene: EDN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12292265_12292266delinsTG , CM000668.2:g.12292265_12292266delinsTG	GRCh38
NC_000006.11:g.12292498_12292499delinsTG , CM000668.1:g.12292498_12292499delinsTG	GRCh37
NC_000006.10:g.12400484_12400485delinsTG	NCBI36
NG_016196.1:g.6970_6971delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379375.6:c.65-76_65-75delinsTG MANE Select	ENSP00000368683.5:n.65-76_65-75delinsTG
ENST00000379375.5:c.65-76_65-75delinsTG	ENSP00000368683.5:n.65-76_65-75delinsTG
NM_001168319.1:c.65-79_65-78delinsTG	NP_001161791.1:n.65-79_65-78delinsTG
NM_001955.4:c.65-76_65-75delinsTG	NP_001946.3:n.65-76_65-75delinsTG
XM_011514330.1:c.65-76_65-75delinsTG	XP_011512632.1:n.65-76_65-75delinsTG
XM_011514331.1:c.65-76_65-75delinsTG	XP_011512633.1:n.65-76_65-75delinsTG
XM_011514332.1:c.65-79_65-78delinsTG	XP_011512634.1:n.65-79_65-78delinsTG
XM_011514330.2:c.65-76_65-75delinsTG	XP_011512632.1:n.65-76_65-75delinsTG
XM_011514331.3:c.65-76_65-75delinsTG	XP_011512633.1:n.65-76_65-75delinsTG
XM_011514332.2:c.65-79_65-78delinsTG	XP_011512634.1:n.65-79_65-78delinsTG
XM_017010331.1:c.65-76_65-75delinsTG	XP_016865820.1:n.65-76_65-75delinsTG
NM_001955.5:c.65-76_65-75delinsTG MANE Select	NP_001946.3:n.65-76_65-75delinsTG
NM_001168319.2:c.65-79_65-78delinsTG	NP_001161791.1:n.65-79_65-78delinsTG