Canonical Allele Identifier: CA1610841644

Gene: EDN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12290514_12290516delinsAAG , CM000668.2:g.12290514_12290516delinsAAG	GRCh38
NC_000006.11:g.12290747_12290749delinsAAG , CM000668.1:g.12290747_12290749delinsAAG	GRCh37
NC_000006.10:g.12398733_12398735delinsAAG	NCBI36
NG_016196.1:g.5219_5221delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379375.6:c.-116_-114delinsAAG MANE Select	ENSP00000368683.5:n.-116_-114delinsAAG
ENST00000379375.5:c.-116_-114delinsAAG	ENSP00000368683.5:n.-116_-114delinsAAG
NM_001168319.1:c.-116_-114delinsAAG	NP_001161791.1:n.-116_-114delinsAAG
NM_001955.4:c.-116_-114delinsAAG	NP_001946.3:n.-116_-114delinsAAG
XM_011514330.1:c.-1-115_-1-113delinsAAG	XP_011512632.1:n.-1-115_-1-113delinsAAG
XM_011514331.1:c.-1-115_-1-113delinsAAG	XP_011512633.1:n.-1-115_-1-113delinsAAG
XM_011514332.1:c.-1-115_-1-113delinsAAG	XP_011512634.1:n.-1-115_-1-113delinsAAG
XM_011514330.2:c.-1-115_-1-113delinsAAG	XP_011512632.1:n.-1-115_-1-113delinsAAG
XM_011514331.3:c.-1-115_-1-113delinsAAG	XP_011512633.1:n.-1-115_-1-113delinsAAG
XM_011514332.2:c.-1-115_-1-113delinsAAG	XP_011512634.1:n.-1-115_-1-113delinsAAG
XM_017010331.1:c.-1-115_-1-113delinsAAG	XP_016865820.1:n.-1-115_-1-113delinsAAG
NM_001955.5:c.-116_-114delinsAAG MANE Select	NP_001946.3:n.-116_-114delinsAAG
NM_001168319.2:c.-116_-114delinsAAG	NP_001161791.1:n.-116_-114delinsAAG