Canonical Allele Identifier: CA1610844321

Gene: EDN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12292609_12292612delinsCCTT , CM000668.2:g.12292609_12292612delinsCCTT	GRCh38
NC_000006.11:g.12292842_12292845delinsCCTT , CM000668.1:g.12292842_12292845delinsCCTT	GRCh37
NC_000006.10:g.12400828_12400831delinsCCTT	NCBI36
NG_016196.1:g.7314_7317delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379375.6:c.233+100_233+103delinsCCTT MANE Select	ENSP00000368683.5:n.233+100_233+103delinsCCTT
ENST00000379375.5:c.233+100_233+103delinsCCTT	ENSP00000368683.5:n.233+100_233+103delinsCCTT
NM_001168319.1:c.230+100_230+103delinsCCTT	NP_001161791.1:n.230+100_230+103delinsCCTT
NM_001955.4:c.233+100_233+103delinsCCTT	NP_001946.3:n.233+100_233+103delinsCCTT
XM_011514330.1:c.233+100_233+103delinsCCTT	XP_011512632.1:n.233+100_233+103delinsCCTT
XM_011514331.1:c.233+100_233+103delinsCCTT	XP_011512633.1:n.233+100_233+103delinsCCTT
XM_011514332.1:c.230+100_230+103delinsCCTT	XP_011512634.1:n.230+100_230+103delinsCCTT
XM_011514330.2:c.233+100_233+103delinsCCTT	XP_011512632.1:n.233+100_233+103delinsCCTT
XM_011514331.3:c.233+100_233+103delinsCCTT	XP_011512633.1:n.233+100_233+103delinsCCTT
XM_011514332.2:c.230+100_230+103delinsCCTT	XP_011512634.1:n.230+100_230+103delinsCCTT
XM_017010331.1:c.233+100_233+103delinsCCTT	XP_016865820.1:n.233+100_233+103delinsCCTT
NM_001955.5:c.233+100_233+103delinsCCTT MANE Select	NP_001946.3:n.233+100_233+103delinsCCTT
NM_001168319.2:c.230+100_230+103delinsCCTT	NP_001161791.1:n.230+100_230+103delinsCCTT