Canonical Allele Identifier: CA353501243
Gene: PROK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.71834113T>G (hg19) chr3:g.71784962T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.71784962T>G , CM000665.2:g.71784962T>G GRCh38
NC_000003.11:g.71834113T>G , CM000665.1:g.71834113T>G GRCh37
NC_000003.10:g.71916803T>G NCBI36
NG_008275.1:g.5245A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295619.4:c.91A>C MANE Select ENSP00000295619.3:p.Thr31Pro
ENST00000295619.3:c.91A>C ENSP00000295619.3:p.Thr31Pro
ENST00000353065.7:c.91A>C ENSP00000295618.3:p.Thr31Pro
NM_001126128.1:c.91A>C NP_001119600.1:p.Thr31Pro
NM_021935.3:c.91A>C NP_068754.1:p.Thr31Pro
NM_001126128.2:c.91A>C MANE Select NP_001119600.1:p.Thr31Pro
NM_021935.4:c.91A>C NP_068754.1:p.Thr31Pro
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