Canonical Allele Identifier: CA2497038049
Gene: PROK2 HGNC NCBI

Linked Data

dbSNP Id: rs2050198334

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.71784773_71784798del , CM000665.2:g.71784773_71784798del GRCh38
NC_000003.11:g.71833924_71833949del , CM000665.1:g.71833924_71833949del GRCh37
NC_000003.10:g.71916614_71916639del NCBI36
NG_008275.1:g.5409_5434del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295619.4:c.96+159_96+184del MANE Select ENSP00000295619.3:n.96+159_96+184del
ENST00000295619.3:c.96+159_96+184del ENSP00000295619.3:n.96+159_96+184del
ENST00000353065.7:c.96+159_96+184del ENSP00000295618.3:n.96+159_96+184del
NM_001126128.1:c.96+159_96+184del NP_001119600.1:n.96+159_96+184del
NM_021935.3:c.96+159_96+184del NP_068754.1:n.96+159_96+184del
NM_001126128.2:c.96+159_96+184del MANE Select NP_001119600.1:n.96+159_96+184del
NM_021935.4:c.96+159_96+184del NP_068754.1:n.96+159_96+184del