Canonical Allele Identifier: CA1502100435

Gene: EDNRA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.147539885T= , CM000666.2:g.147539885T=	GRCh38
NC_000004.11:g.148461037T= , CM000666.1:g.148461037T=	GRCh37
NC_000004.10:g.148680487T=	NCBI36
NG_013343.1:g.63969T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001957.4:c.969T= MANE Select	NP_001948.1:p.His323=
ENST00000651419.1:c.969T= MANE Select	ENSP00000498969.1:p.His323=
NM_001166055.1:c.642T=	NP_001159527.1:p.His214=
NM_001166055.2:c.642T=	NP_001159527.1:p.His214=
NM_001256283.1:c.294T=	NP_001243212.1:p.His98=
NM_001957.3:c.969T=	NP_001948.1:p.His323=
NR_045958.1:n.1300T=
NR_045958.2:n.1120T=
NR_148963.1:n.1009T=
NR_148963.2:n.829T=
NR_148964.1:n.810T=
NR_148964.2:n.630T=
ENST00000324300.10:c.969T=	ENSP00000315011.5:p.His323=
ENST00000324300.9:c.969T=	ENSP00000315011.5:p.His323=
ENST00000358556.8:c.642T=	ENSP00000351359.4:p.His214=
ENST00000503721.1:n.509T=
ENST00000506066.1:c.642T=	ENSP00000425281.1:p.His214=
ENST00000510697.5:c.770T=	ENSP00000427259.1:n.770T=
ENST00000511804.5:c.294T=	ENSP00000425354.1:p.His98=
ENST00000648866.1:c.294T=	ENSP00000496976.1:p.His98=