Canonical Allele Identifier: CA11735776

Gene: EDNRA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.147539638C>G , CM000666.2:g.147539638C>G	GRCh38
NC_000004.11:g.148460790C>G , CM000666.1:g.148460790C>G	GRCh37
NC_000004.10:g.148680240C>G	NCBI36
NG_013343.1:g.63722C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001957.4:c.901-179C>G MANE Select	NP_001948.1:n.901-179C>G
ENST00000651419.1:c.901-179C>G MANE Select	ENSP00000498969.1:n.901-179C>G
NM_001166055.1:c.574-179C>G	NP_001159527.1:n.574-179C>G
NM_001166055.2:c.574-179C>G	NP_001159527.1:n.574-179C>G
NM_001256283.1:c.226-179C>G	NP_001243212.1:n.226-179C>G
NM_001957.3:c.901-179C>G	NP_001948.1:n.901-179C>G
NR_045958.1:n.1232-179C>G
NR_045958.2:n.1052-179C>G
NR_148963.1:n.941-179C>G
NR_148963.2:n.761-179C>G
NR_148964.1:n.742-179C>G
NR_148964.2:n.562-179C>G
ENST00000324300.10:c.901-179C>G	ENSP00000315011.5:n.901-179C>G
ENST00000324300.9:c.901-179C>G	ENSP00000315011.5:n.901-179C>G
ENST00000358556.8:c.574-179C>G	ENSP00000351359.4:n.574-179C>G
ENST00000503721.1:n.441-179C>G
ENST00000506066.1:c.574-179C>G	ENSP00000425281.1:n.574-179C>G
ENST00000510697.5:c.702-179C>G	ENSP00000427259.1:n.702-179C>G
ENST00000511804.5:c.226-179C>G	ENSP00000425354.1:n.226-179C>G
ENST00000648866.1:c.226-179C>G	ENSP00000496976.1:n.226-179C>G