Canonical Allele Identifier: CA1610843513

Gene: EDN1

Linked Data

• dbSNP Id: rs1762700024

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12292202_12292203insGC , CM000668.2:g.12292202_12292203insGC	GRCh38
NC_000006.11:g.12292435_12292436insGC , CM000668.1:g.12292435_12292436insGC	GRCh37
NC_000006.10:g.12400421_12400422insGC	NCBI36
NG_016196.1:g.6907_6908insGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000379375.6:c.65-139_65-138insGC MANE Select	ENSP00000368683.5:n.65-139_65-138insGC
ENST00000379375.5:c.65-139_65-138insGC	ENSP00000368683.5:n.65-139_65-138insGC
NM_001168319.1:c.65-142_65-141insGC	NP_001161791.1:n.65-142_65-141insGC
NM_001955.4:c.65-139_65-138insGC	NP_001946.3:n.65-139_65-138insGC
XM_011514330.1:c.65-139_65-138insGC	XP_011512632.1:n.65-139_65-138insGC
XM_011514331.1:c.65-139_65-138insGC	XP_011512633.1:n.65-139_65-138insGC
XM_011514332.1:c.65-142_65-141insGC	XP_011512634.1:n.65-142_65-141insGC
XM_011514330.2:c.65-139_65-138insGC	XP_011512632.1:n.65-139_65-138insGC
XM_011514331.3:c.65-139_65-138insGC	XP_011512633.1:n.65-139_65-138insGC
XM_011514332.2:c.65-142_65-141insGC	XP_011512634.1:n.65-142_65-141insGC
XM_017010331.1:c.65-139_65-138insGC	XP_016865820.1:n.65-139_65-138insGC
NM_001955.5:c.65-139_65-138insGC MANE Select	NP_001946.3:n.65-139_65-138insGC
NM_001168319.2:c.65-142_65-141insGC	NP_001161791.1:n.65-142_65-141insGC