Canonical Allele Identifier: CA532302605
Gene: EPAS1 HGNC NCBI

Linked Data

dbSNP Id: rs1360203277

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.46350251_46350261del , CM000664.2:g.46350251_46350261del GRCh38
NC_000002.11:g.46577390_46577400del , CM000664.1:g.46577390_46577400del GRCh37
NC_000002.10:g.46430894_46430904del NCBI36
NG_016000.1:g.57850_57860del

Transcript Alleles

HGVS Amino-acid change
ENST00000263734.5:c.217+3188_217+3198del MANE Select ENSP00000263734.3:n.217+3188_217+3198del
ENST00000263734.4:c.217+3188_217+3198del ENSP00000263734.3:n.217+3188_217+3198del
ENST00000449347.5:c.217+3188_217+3198del ENSP00000406137.1:n.217+3188_217+3198del
ENST00000475822.1:n.408+3188_408+3198del
NM_001430.4:c.217+3188_217+3198del NP_001421.2:n.217+3188_217+3198del
XM_011532698.1:c.256+3188_256+3198del XP_011531000.1:n.256+3188_256+3198del
XM_011532698.2:c.256+3188_256+3198del XP_011531000.1:n.256+3188_256+3198del
NM_001430.5:c.217+3188_217+3198del MANE Select NP_001421.2:n.217+3188_217+3198del