Canonical Allele Identifier: CA2625696129
Gene: PROX2 HGNC NCBI
YLPM1 HGNC NCBI

Linked Data

gnomAD v4: 14-74855017-GA-G
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000556489.4:c.*114del (PROX2) MANE Select ENSP00000451223.2:n.*114del
ENST00000673765.1:c.*114del (PROX2) ENSP00000501015.1:n.*114del
ENST00000553381.1:n.238-199del (YLPM1)
ENST00000554107.2:c.206-199del (YLPM1)
ENST00000556084.6:c.1212del (PROX2) ENSP00000451463.2:n.1212del
ENST00000556489.3:c.1893del (PROX2) ENSP00000451223.2:n.1893del
NM_001080408.2:c.1212del (PROX2) NP_001073877.2:n.1212del
NM_001243007.1:c.1893del (PROX2) NP_001229936.1:n.1893del
XM_005267543.2:c.*114del (PROX2) XP_005267600.1:n.*114del
NM_001080408.3:c.*114del (PROX2) NP_001073877.2:n.*114del
NM_001243007.2:c.*114del (PROX2) MANE Select NP_001229936.1:n.*114del
NM_001384314.1:c.*114del (PROX2) NP_001371243.1:n.*114del
NR_169190.1:n.2518del (PROX2)
Search 100 bp 5'
Search 100 bp 3'