Canonical Allele Identifier: CA46520181

Gene: EPAS1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.46331069T>A , CM000664.2:g.46331069T>A	GRCh38
NC_000002.11:g.46558208T>A , CM000664.1:g.46558208T>A	GRCh37
NC_000002.10:g.46411712T>A	NCBI36
NG_016000.1:g.38668T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263734.5:c.27-15804T>A MANE Select	ENSP00000263734.3:n.27-15804T>A
ENST00000263734.4:c.27-15804T>A	ENSP00000263734.3:n.27-15804T>A
ENST00000449347.5:c.27-15804T>A	ENSP00000406137.1:n.27-15804T>A
ENST00000460015.1:n.433-15804T>A
ENST00000467888.5:n.175-15804T>A
NM_001430.4:c.27-15804T>A	NP_001421.2:n.27-15804T>A
XM_011532698.1:c.65+5193T>A	XP_011531000.1:n.65+5193T>A
XR_940055.1:n.2355+4715A>T
XM_011532698.2:c.65+5193T>A	XP_011531000.1:n.65+5193T>A
NM_001430.5:c.27-15804T>A MANE Select	NP_001421.2:n.27-15804T>A