Canonical Allele Identifier: CA2666513413
Gene: PROK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.71784897del , CM000665.2:g.71784897del GRCh38
NC_000003.11:g.71834048del , CM000665.1:g.71834048del GRCh37
NC_000003.10:g.71916738del NCBI36
NG_008275.1:g.5310del

Transcript Alleles

HGVS Amino-acid change
ENST00000295619.4:c.96+60del MANE Select ENSP00000295619.3:n.96+60del
ENST00000295619.3:c.96+60del ENSP00000295619.3:n.96+60del
ENST00000353065.7:c.96+60del ENSP00000295618.3:n.96+60del
NM_001126128.1:c.96+60del NP_001119600.1:n.96+60del
NM_021935.3:c.96+60del NP_068754.1:n.96+60del
NM_001126128.2:c.96+60del MANE Select NP_001119600.1:n.96+60del
NM_021935.4:c.96+60del NP_068754.1:n.96+60del