Canonical Allele Identifier: CA910039500
Gene: PROK2 HGNC NCBI

Linked Data

dbSNP Id: rs1393841777

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.71784823_71784824insT , CM000665.2:g.71784823_71784824insT GRCh38
NC_000003.11:g.71833974_71833975insT , CM000665.1:g.71833974_71833975insT GRCh37
NC_000003.10:g.71916664_71916665insT NCBI36
NG_008275.1:g.5383_5384insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000295619.4:c.96+133_96+134insA MANE Select ENSP00000295619.3:n.96+133_96+134insA
ENST00000295619.3:c.96+133_96+134insA ENSP00000295619.3:n.96+133_96+134insA
ENST00000353065.7:c.96+133_96+134insA ENSP00000295618.3:n.96+133_96+134insA
NM_001126128.1:c.96+133_96+134insA NP_001119600.1:n.96+133_96+134insA
NM_021935.3:c.96+133_96+134insA NP_068754.1:n.96+133_96+134insA
NM_001126128.2:c.96+133_96+134insA MANE Select NP_001119600.1:n.96+133_96+134insA
NM_021935.4:c.96+133_96+134insA NP_068754.1:n.96+133_96+134insA