Canonical Allele Identifier: CA2844148858
Gene: EPAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.46329183A>T , CM000664.2:g.46329183A>T GRCh38
NC_000002.11:g.46556322A>T , CM000664.1:g.46556322A>T GRCh37
NC_000002.10:g.46409826A>T NCBI36
NG_016000.1:g.36782A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263734.5:c.27-17690A>T MANE Select ENSP00000263734.3:n.27-17690A>T
ENST00000263734.4:c.27-17690A>T ENSP00000263734.3:n.27-17690A>T
ENST00000449347.5:c.27-17690A>T ENSP00000406137.1:n.27-17690A>T
ENST00000460015.1:n.433-17690A>T
ENST00000467888.5:n.175-17690A>T
NM_001430.4:c.27-17690A>T NP_001421.2:n.27-17690A>T
XM_011532698.1:c.65+3307A>T XP_011531000.1:n.65+3307A>T
XR_940055.1:n.2355+6601T>A
XM_011532698.2:c.65+3307A>T XP_011531000.1:n.65+3307A>T
NM_001430.5:c.27-17690A>T MANE Select NP_001421.2:n.27-17690A>T