Canonical Allele Identifier: CA1610830999

Gene: EDN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12296046_12296056delinsCCACAACCGAG , CM000668.2:g.12296046_12296056delinsCCACAACCGAG	GRCh38
NC_000006.11:g.12296279_12296289delinsCCACAACCGAG , CM000668.1:g.12296279_12296289delinsCCACAACCGAG	GRCh37
NC_000006.10:g.12404265_12404275delinsCCACAACCGAG	NCBI36
NG_016196.1:g.10751_10761delinsCCACAACCGAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000379375.6:c.618_628delinsCCACAACCGAG MANE Select	ENSP00000368683.5:p.Thr206=
ENST00000379375.5:c.618_628delinsCCACAACCGAG	ENSP00000368683.5:p.Thr206=
NM_001168319.1:c.615_625delinsCCACAACCGAG	NP_001161791.1:p.Thr205=
NM_001955.4:c.618_628delinsCCACAACCGAG	NP_001946.3:p.Thr206=
XM_011514330.1:c.618_628delinsCCACAACCGAG	XP_011512632.1:p.Thr206=
XM_011514331.1:c.618_628delinsCCACAACCGAG	XP_011512633.1:p.Thr206=
XM_011514332.1:c.615_625delinsCCACAACCGAG	XP_011512634.1:p.Thr205=
XM_011514330.2:c.618_628delinsCCACAACCGAG	XP_011512632.1:p.Thr206=
XM_011514331.3:c.618_628delinsCCACAACCGAG	XP_011512633.1:p.Thr206=
XM_011514332.2:c.615_625delinsCCACAACCGAG	XP_011512634.1:p.Thr205=
XM_017010331.1:c.618_628delinsCCACAACCGAG	XP_016865820.1:p.Thr206=
NM_001955.5:c.618_628delinsCCACAACCGAG MANE Select	NP_001946.3:p.Thr206=
NM_001168319.2:c.615_625delinsCCACAACCGAG	NP_001161791.1:p.Thr205=