Canonical Allele Identifier: CA2495266802

Gene: EPAS1

Linked Data

• dbSNP Id: rs1684120857

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.46350229_46350230del , CM000664.2:g.46350229_46350230del	GRCh38
NC_000002.11:g.46577368_46577369del , CM000664.1:g.46577368_46577369del	GRCh37
NC_000002.10:g.46430872_46430873del	NCBI36
NG_016000.1:g.57828_57829del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263734.5:c.217+3166_217+3167del MANE Select	ENSP00000263734.3:n.217+3166_217+3167del
ENST00000263734.4:c.217+3166_217+3167del	ENSP00000263734.3:n.217+3166_217+3167del
ENST00000449347.5:c.217+3166_217+3167del	ENSP00000406137.1:n.217+3166_217+3167del
ENST00000475822.1:n.408+3166_408+3167del
NM_001430.4:c.217+3166_217+3167del	NP_001421.2:n.217+3166_217+3167del
XM_011532698.1:c.256+3166_256+3167del	XP_011531000.1:n.256+3166_256+3167del
XM_011532698.2:c.256+3166_256+3167del	XP_011531000.1:n.256+3166_256+3167del
NM_001430.5:c.217+3166_217+3167del MANE Select	NP_001421.2:n.217+3166_217+3167del