Canonical Allele Identifier: CA409707105

Gene: EDN3

Linked Data

• MyVariant Identifiers: chr20:g.57876743T>C (hg19) ; chr20:g.59301688T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.59301688T>C , CM000682.2:g.59301688T>C	GRCh38
NC_000020.10:g.57876743T>C , CM000682.1:g.57876743T>C	GRCh37
NC_000020.9:g.57310138T>C	NCBI36
NG_008050.1:g.6245T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337938.7:c.331T>C MANE Select	ENSP00000337128.2:p.Cys111Arg
ENST00000644821.1:c.331T>C	ENSP00000493472.1:p.Cys111Arg
ENST00000671744.1:n.972T>C
ENST00000672969.1:c.168T>C
ENST00000311585.11:c.331T>C	ENSP00000311854.7:p.Cys111Arg
ENST00000337938.6:c.331T>C	ENSP00000337128.2:p.Cys111Arg
ENST00000371025.7:c.331T>C	ENSP00000360064.3:p.Cys111Arg
ENST00000371028.6:c.331T>C	ENSP00000360067.2:p.Cys111Arg
ENST00000395654.3:c.331T>C	ENSP00000379015.3:p.Cys111Arg
NM_001302455.1:c.331T>C	NP_001289384.1:p.Cys111Arg
NM_001302456.1:c.331T>C	NP_001289385.1:p.Cys111Arg
NM_207032.2:c.331T>C	NP_996915.1:p.Cys111Arg
NM_207033.2:c.331T>C	NP_996916.1:p.Cys111Arg
NM_207034.2:c.331T>C	NP_996917.1:p.Cys111Arg
XM_005260312.3:c.331T>C	XP_005260369.1:p.Cys111Arg
XM_005260313.3:c.331T>C	XP_005260370.1:p.Cys111Arg
XM_006723734.2:c.331T>C	XP_006723797.1:p.Cys111Arg
XM_011528655.1:c.331T>C	XP_011526957.1:p.Cys111Arg
XR_936513.1:n.720T>C
XM_005260312.4:c.331T>C	XP_005260369.1:p.Cys111Arg
XM_005260313.5:c.331T>C	XP_005260370.1:p.Cys111Arg
XM_006723734.3:c.331T>C	XP_006723797.1:p.Cys111Arg
XM_011528655.2:c.331T>C	XP_011526957.1:p.Cys111Arg
XM_024451847.1:c.331T>C	XP_024307615.1:p.Cys111Arg
XM_024451848.1:c.331T>C	XP_024307616.1:p.Cys111Arg
XR_002958461.1:n.729T>C
XR_002958462.1:n.729T>C
XR_936513.2:n.728T>C
NM_207034.3:c.331T>C MANE Select	NP_996917.1:p.Cys111Arg
NM_001302455.2:c.331T>C	NP_001289384.1:p.Cys111Arg
NM_001302456.2:c.331T>C	NP_001289385.1:p.Cys111Arg
NM_207032.3:c.331T>C	NP_996915.1:p.Cys111Arg
NM_207033.3:c.331T>C	NP_996916.1:p.Cys111Arg