Canonical Allele Identifier: CA2147230580

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74854918C= , CM000676.2:g.74854918C= GRCh38
NC_000014.8:g.75321621C= , CM000676.1:g.75321621C= GRCh37
NC_000014.7:g.74391374C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000556489.4:c.*214G= (PROX2) MANE Select ENSP00000451223.2:n.*214G=
ENST00000673765.1:c.*214G= (PROX2) ENSP00000501015.1:n.*214G=
ENST00000553381.1:n.238-299C= (YLPM1)
ENST00000554107.2:c.206-299C= (YLPM1)
ENST00000556084.6:c.1312G= (PROX2) ENSP00000451463.2:n.1312G=
ENST00000556489.3:c.1993G= (PROX2) ENSP00000451223.2:n.1993G=
NM_001080408.2:c.1312G= (PROX2) NP_001073877.2:n.1312G=
NM_001243007.1:c.1993G= (PROX2) NP_001229936.1:n.1993G=
XM_005267543.2:c.*214G= (PROX2) XP_005267600.1:n.*214G=
NM_001080408.3:c.*214G= (PROX2) NP_001073877.2:n.*214G=
NM_001243007.2:c.*214G= (PROX2) MANE Select NP_001229936.1:n.*214G=
NM_001384314.1:c.*214G= (PROX2) NP_001371243.1:n.*214G=
NR_169190.1:n.2618G= (PROX2)