Canonical Allele Identifier: CA3098037

Gene: EDNRA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.147540452T>C , CM000666.2:g.147540452T>C	GRCh38
NC_000004.11:g.148461604T>C , CM000666.1:g.148461604T>C	GRCh37
NC_000004.10:g.148681054T>C	NCBI36
NG_013343.1:g.64536T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324300.10:c.1110T>C	ENSP00000315011.5:p.Tyr370=
ENST00000648866.1:c.435T>C	ENSP00000496976.1:p.Tyr145=
ENST00000651419.1:c.1110T>C MANE Select	ENSP00000498969.1:p.Tyr370=
ENST00000324300.9:c.1110T>C	ENSP00000315011.5:p.Tyr370=
ENST00000358556.8:c.783T>C	ENSP00000351359.4:p.Tyr261=
ENST00000503721.1:n.650T>C
ENST00000506066.1:c.783T>C	ENSP00000425281.1:p.Tyr261=
ENST00000510697.5:c.911T>C	ENSP00000427259.1:n.911T>C
ENST00000511804.5:c.435T>C	ENSP00000425354.1:p.Tyr145=
NM_001166055.1:c.783T>C	NP_001159527.1:p.Tyr261=
NM_001256283.1:c.435T>C	NP_001243212.1:p.Tyr145=
NM_001957.3:c.1110T>C	NP_001948.1:p.Tyr370=
NR_045958.1:n.1441T>C
NR_148963.1:n.1150T>C
NR_148964.1:n.951T>C
NM_001957.4:c.1110T>C MANE Select	NP_001948.1:p.Tyr370=
NR_045958.2:n.1261T>C
NR_148963.2:n.970T>C
NR_148964.2:n.771T>C
NM_001166055.2:c.783T>C	NP_001159527.1:p.Tyr261=