Canonical Allele Identifier: CA2147230615

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74855018A= , CM000676.2:g.74855018A= GRCh38
NC_000014.8:g.75321721A= , CM000676.1:g.75321721A= GRCh37
NC_000014.7:g.74391474A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000556489.4:c.*114T= (PROX2) MANE Select ENSP00000451223.2:n.*114T=
ENST00000673765.1:c.*114T= (PROX2) ENSP00000501015.1:n.*114T=
ENST00000553381.1:n.238-199A= (YLPM1)
ENST00000554107.2:c.206-199A= (YLPM1)
ENST00000556084.6:c.1212T= (PROX2) ENSP00000451463.2:n.1212T=
ENST00000556489.3:c.1893T= (PROX2) ENSP00000451223.2:n.1893T=
NM_001080408.2:c.1212T= (PROX2) NP_001073877.2:n.1212T=
NM_001243007.1:c.1893T= (PROX2) NP_001229936.1:n.1893T=
XM_005267543.2:c.*114T= (PROX2) XP_005267600.1:n.*114T=
NM_001080408.3:c.*114T= (PROX2) NP_001073877.2:n.*114T=
NM_001243007.2:c.*114T= (PROX2) MANE Select NP_001229936.1:n.*114T=
NM_001384314.1:c.*114T= (PROX2) NP_001371243.1:n.*114T=
NR_169190.1:n.2518T= (PROX2)