Canonical Allele Identifier: CA362856956

Gene: EDN1

Linked Data

• gnomAD v4: 6-12294295-C-A
• MyVariant Identifiers: chr6:g.12294528C>A (hg19) ; chr6:g.12294295C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12294295C>A , CM000668.2:g.12294295C>A	GRCh38
NC_000006.11:g.12294528C>A , CM000668.1:g.12294528C>A	GRCh37
NC_000006.10:g.12402514C>A	NCBI36
NG_016196.1:g.9000C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379375.6:c.424C>A MANE Select	ENSP00000368683.5:p.His142Asn
ENST00000379375.5:c.424C>A	ENSP00000368683.5:p.His142Asn
NM_001168319.1:c.421C>A	NP_001161791.1:p.His141Asn
NM_001955.4:c.424C>A	NP_001946.3:p.His142Asn
XM_011514330.1:c.424C>A	XP_011512632.1:p.His142Asn
XM_011514331.1:c.424C>A	XP_011512633.1:p.His142Asn
XM_011514332.1:c.421C>A	XP_011512634.1:p.His141Asn
XM_011514330.2:c.424C>A	XP_011512632.1:p.His142Asn
XM_011514331.3:c.424C>A	XP_011512633.1:p.His142Asn
XM_011514332.2:c.421C>A	XP_011512634.1:p.His141Asn
XM_017010331.1:c.424C>A	XP_016865820.1:p.His142Asn
NM_001955.5:c.424C>A MANE Select	NP_001946.3:p.His142Asn
NM_001168319.2:c.421C>A	NP_001161791.1:p.His141Asn