Canonical Allele Identifier: CA1139790697
Gene: PROX1 HGNC NCBI
PROX1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213985913T= , CM000663.2:g.213985913T= GRCh38
NC_000001.10:g.214159256T= , CM000663.1:g.214159256T= GRCh37
NC_000001.9:g.212225879T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000471129.1:c.-68+2590T= (PROX1) ENSP00000419517.1:n.-68+2590T=
NR_037850.2:n.85+156A= (PROX1-AS1)
XM_011509773.1:c.-68+2590T= (PROX1) XP_011508075.1:n.-68+2590T=
XM_011509773.2:c.-68+2590T= (PROX1) XP_011508075.1:n.-68+2590T=