Canonical Allele Identifier: CA1502049458
Gene: EDNRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.147526161G= , CM000666.2:g.147526161G= GRCh38
NC_000004.11:g.148447313G= , CM000666.1:g.148447313G= GRCh37
NC_000004.10:g.148666763G= NCBI36
NG_013343.1:g.50245G=

Transcript Alleles

HGVS Amino-acid change
ENST00000324300.10:c.548+6183G= ENSP00000315011.5:n.548+6183G=
ENST00000648866.1:c.-128+6183G= ENSP00000496976.1:n.-128+6183G=
ENST00000651419.1:c.548+6183G= MANE Select ENSP00000498969.1:n.548+6183G=
ENST00000324300.9:c.548+6183G= ENSP00000315011.5:n.548+6183G=
ENST00000358556.8:c.421-9716G= ENSP00000351359.4:n.421-9716G=
ENST00000506066.1:c.421-9716G= ENSP00000425281.1:n.421-9716G=
ENST00000510697.5:c.548+6183G= ENSP00000427259.1:n.548+6183G=
ENST00000511804.5:c.-128+6183G= ENSP00000425354.1:n.-128+6183G=
ENST00000514245.1:n.269-6345G=
NM_001166055.1:c.421-9716G= NP_001159527.1:n.421-9716G=
NM_001256283.1:c.-128+6183G= NP_001243212.1:n.-128+6183G=
NM_001957.3:c.548+6183G= NP_001948.1:n.548+6183G=
NR_045958.1:n.1078+6183G=
NM_001354797.1:c.549-336G= NP_001341726.1:n.549-336G=
NR_148963.1:n.588+6183G=
NR_148964.1:n.588+6183G=
NM_001957.4:c.548+6183G= MANE Select NP_001948.1:n.548+6183G=
NM_001354797.2:c.549-336G= NP_001341726.1:n.549-336G=
NR_045958.2:n.898+6183G=
NR_148963.2:n.408+6183G=
NR_148964.2:n.408+6183G=
NM_001166055.2:c.421-9716G= NP_001159527.1:n.421-9716G=