Canonical Allele Identifier: CA362857056

Gene: EDN1

Linked Data

• MyVariant Identifiers: chr6:g.12294571T>G (hg19) ; chr6:g.12294338T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12294338T>G , CM000668.2:g.12294338T>G	GRCh38
NC_000006.11:g.12294571T>G , CM000668.1:g.12294571T>G	GRCh37
NC_000006.10:g.12402557T>G	NCBI36
NG_016196.1:g.9043T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379375.6:c.467T>G MANE Select	ENSP00000368683.5:p.Ile156Ser
ENST00000379375.5:c.467T>G	ENSP00000368683.5:p.Ile156Ser
NM_001168319.1:c.464T>G	NP_001161791.1:p.Ile155Ser
NM_001955.4:c.467T>G	NP_001946.3:p.Ile156Ser
XM_011514330.1:c.467T>G	XP_011512632.1:p.Ile156Ser
XM_011514331.1:c.467T>G	XP_011512633.1:p.Ile156Ser
XM_011514332.1:c.464T>G	XP_011512634.1:p.Ile155Ser
XM_011514330.2:c.467T>G	XP_011512632.1:p.Ile156Ser
XM_011514331.3:c.467T>G	XP_011512633.1:p.Ile156Ser
XM_011514332.2:c.464T>G	XP_011512634.1:p.Ile155Ser
XM_017010331.1:c.467T>G	XP_016865820.1:p.Ile156Ser
NM_001955.5:c.467T>G MANE Select	NP_001946.3:p.Ile156Ser
NM_001168319.2:c.464T>G	NP_001161791.1:p.Ile155Ser