Canonical Allele Identifier: CA1610831449

Gene: EDN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12296502_12296503delinsCA , CM000668.2:g.12296502_12296503delinsCA	GRCh38
NC_000006.11:g.12296735_12296736delinsCA , CM000668.1:g.12296735_12296736delinsCA	GRCh37
NC_000006.10:g.12404721_12404722delinsCA	NCBI36
NG_016196.1:g.11207_11208delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379375.6:c.*435_*436delinsCA MANE Select	ENSP00000368683.5:n.*435_*436delinsCA
ENST00000379375.5:c.*435_*436delinsCA	ENSP00000368683.5:n.*435_*436delinsCA
NM_001168319.1:c.*435_*436delinsCA	NP_001161791.1:n.*435_*436delinsCA
NM_001955.4:c.*435_*436delinsCA	NP_001946.3:n.*435_*436delinsCA
XM_011514330.1:c.*435_*436delinsCA	XP_011512632.1:n.*435_*436delinsCA
XM_011514331.1:c.*435_*436delinsCA	XP_011512633.1:n.*435_*436delinsCA
XM_011514332.1:c.*435_*436delinsCA	XP_011512634.1:n.*435_*436delinsCA
XM_011514330.2:c.*435_*436delinsCA	XP_011512632.1:n.*435_*436delinsCA
XM_011514331.3:c.*435_*436delinsCA	XP_011512633.1:n.*435_*436delinsCA
XM_011514332.2:c.*435_*436delinsCA	XP_011512634.1:n.*435_*436delinsCA
XM_017010331.1:c.*435_*436delinsCA	XP_016865820.1:n.*435_*436delinsCA
NM_001955.5:c.*435_*436delinsCA MANE Select	NP_001946.3:n.*435_*436delinsCA
NM_001168319.2:c.*435_*436delinsCA	NP_001161791.1:n.*435_*436delinsCA