Canonical Allele Identifier: CA2372704736

Gene: EDN3

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.59301595G= , CM000682.2:g.59301595G=	GRCh38
NC_000020.10:g.57876650G= , CM000682.1:g.57876650G=	GRCh37
NC_000020.9:g.57310045G=	NCBI36
NG_008050.1:g.6152G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000337938.7:c.238G= MANE Select	ENSP00000337128.2:p.Gly80=
ENST00000644821.1:c.238G=	ENSP00000493472.1:p.Gly80=
ENST00000671744.1:n.879G=
ENST00000672969.1:c.75G=
ENST00000311585.11:c.238G=	ENSP00000311854.7:p.Gly80=
ENST00000337938.6:c.238G=	ENSP00000337128.2:p.Gly80=
ENST00000371025.7:c.238G=	ENSP00000360064.3:p.Gly80=
ENST00000371028.6:c.238G=	ENSP00000360067.2:p.Gly80=
ENST00000395654.3:c.238G=	ENSP00000379015.3:p.Gly80=
NM_001302455.1:c.238G=	NP_001289384.1:p.Gly80=
NM_001302456.1:c.238G=	NP_001289385.1:p.Gly80=
NM_207032.2:c.238G=	NP_996915.1:p.Gly80=
NM_207033.2:c.238G=	NP_996916.1:p.Gly80=
NM_207034.2:c.238G=	NP_996917.1:p.Gly80=
XM_005260312.3:c.238G=	XP_005260369.1:p.Gly80=
XM_005260313.3:c.238G=	XP_005260370.1:p.Gly80=
XM_006723734.2:c.238G=	XP_006723797.1:p.Gly80=
XM_011528655.1:c.238G=	XP_011526957.1:p.Gly80=
XR_936513.1:n.627G=
XM_005260312.4:c.238G=	XP_005260369.1:p.Gly80=
XM_005260313.5:c.238G=	XP_005260370.1:p.Gly80=
XM_006723734.3:c.238G=	XP_006723797.1:p.Gly80=
XM_011528655.2:c.238G=	XP_011526957.1:p.Gly80=
XM_024451847.1:c.238G=	XP_024307615.1:p.Gly80=
XM_024451848.1:c.238G=	XP_024307616.1:p.Gly80=
XR_002958461.1:n.636G=
XR_002958462.1:n.636G=
XR_936513.2:n.635G=
NM_207034.3:c.238G= MANE Select	NP_996917.1:p.Gly80=
NM_001302455.2:c.238G=	NP_001289384.1:p.Gly80=
NM_001302456.2:c.238G=	NP_001289385.1:p.Gly80=
NM_207032.3:c.238G=	NP_996915.1:p.Gly80=
NM_207033.3:c.238G=	NP_996916.1:p.Gly80=