Canonical Allele Identifier: CA11837998
Gene: EDNRA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.147530682G>A , CM000666.2:g.147530682G>A GRCh38
NC_000004.11:g.148451834G>A , CM000666.1:g.148451834G>A GRCh37
NC_000004.10:g.148671284G>A NCBI36
NG_013343.1:g.54766G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000324300.10:c.549-1824G>A ENSP00000315011.5:n.549-1824G>A
ENST00000648866.1:c.-127-1824G>A ENSP00000496976.1:n.-127-1824G>A
ENST00000651419.1:c.549-1824G>A MANE Select ENSP00000498969.1:n.549-1824G>A
ENST00000324300.9:c.549-1824G>A ENSP00000315011.5:n.549-1824G>A
ENST00000358556.8:c.421-5195G>A ENSP00000351359.4:n.421-5195G>A
ENST00000506066.1:c.421-5195G>A ENSP00000425281.1:n.421-5195G>A
ENST00000510697.5:c.549-5195G>A ENSP00000427259.1:n.549-5195G>A
ENST00000511804.5:c.-127-1824G>A ENSP00000425354.1:n.-127-1824G>A
ENST00000514245.1:n.269-1824G>A
NM_001166055.1:c.421-5195G>A NP_001159527.1:n.421-5195G>A
NM_001256283.1:c.-127-1824G>A NP_001243212.1:n.-127-1824G>A
NM_001957.3:c.549-1824G>A NP_001948.1:n.549-1824G>A
NR_045958.1:n.1079-5195G>A
NR_148963.1:n.589-1824G>A
NR_148964.1:n.589-5195G>A
NM_001957.4:c.549-1824G>A MANE Select NP_001948.1:n.549-1824G>A
NR_045958.2:n.899-5195G>A
NR_148963.2:n.409-1824G>A
NR_148964.2:n.409-5195G>A
NM_001166055.2:c.421-5195G>A NP_001159527.1:n.421-5195G>A
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