Canonical Allele Identifier: CA2103860764

Gene: EDNRB EDNRB-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.77900995_77900999delinsATAAT , CM000675.2:g.77900995_77900999delinsATAAT	GRCh38
NC_000013.10:g.78475130_78475134delinsATAAT , CM000675.1:g.78475130_78475134delinsATAAT	GRCh37
NC_000013.9:g.77373131_77373135delinsATAAT	NCBI36
NG_011630.2:g.79531_79535delinsATTAT
NG_011630.3:g.78725_78729delinsATTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475537.2:c.951+59_951+63delinsATTAT (EDNRB)	ENSP00000487082.2:n.951+59_951+63delinsATTAT
ENST00000643890.1:c.951+59_951+63delinsATTAT (EDNRB)	ENSP00000495815.1:n.951+59_951+63delinsATTAT
ENST00000645696.1:c.429+59_429+63delinsATTAT (EDNRB)	ENSP00000495984.1:n.429+59_429+63delinsATTAT
ENST00000646605.1:c.951+59_951+63delinsATTAT (EDNRB)	ENSP00000494278.1:n.951+59_951+63delinsATTAT
ENST00000646607.2:c.951+59_951+63delinsATTAT (EDNRB) MANE Select	ENSP00000493527.1:n.951+59_951+63delinsATTAT
ENST00000646948.1:c.951+59_951+63delinsATTAT (EDNRB)	ENSP00000493895.1:n.951+59_951+63delinsATTAT
ENST00000334286.7:c.951+59_951+63delinsATTAT (EDNRB)	ENSP00000335311.5:n.951+59_951+63delinsATTAT
ENST00000377211.8:c.1221+59_1221+63delinsATTAT (EDNRB)	ENSP00000366416.4:n.1221+59_1221+63delinsATTAT
ENST00000626030.1:c.951+59_951+63delinsATTAT (EDNRB)	ENSP00000486202.1:n.951+59_951+63delinsATTAT
NM_000115.3:c.951+59_951+63delinsATTAT (EDNRB)	NP_000106.1:n.951+59_951+63delinsATTAT
NM_001122659.2:c.951+59_951+63delinsATTAT (EDNRB)	NP_001116131.1:n.951+59_951+63delinsATTAT
NM_001201397.1:c.1221+59_1221+63delinsATTAT (EDNRB)	NP_001188326.1:n.1221+59_1221+63delinsATTAT
NM_003991.3:c.951+59_951+63delinsATTAT (EDNRB)	NP_003982.1:n.951+59_951+63delinsATTAT
NR_103853.1:n.1695-6697_1695-6693delinsATAAT (EDNRB-AS1)
XM_005266275.2:c.951+59_951+63delinsATTAT (EDNRB)	XP_005266332.2:n.951+59_951+63delinsATTAT
XM_011534949.1:c.951+59_951+63delinsATTAT (EDNRB)	XP_011533251.1:n.951+59_951+63delinsATTAT
NM_000115.4:c.951+59_951+63delinsATTAT (EDNRB)	NP_000106.1:n.951+59_951+63delinsATTAT
NM_001122659.3:c.951+59_951+63delinsATTAT (EDNRB) MANE Select	NP_001116131.1:n.951+59_951+63delinsATTAT
NM_000115.5:c.951+59_951+63delinsATTAT (EDNRB)	NP_000106.1:n.951+59_951+63delinsATTAT
NM_003991.4:c.951+59_951+63delinsATTAT (EDNRB)	NP_003982.1:n.951+59_951+63delinsATTAT