Canonical Allele Identifier: CA353500970
Gene: PROK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.71830631G>T (hg19) chr3:g.71781480G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.71781480G>T , CM000665.2:g.71781480G>T GRCh38
NC_000003.11:g.71830631G>T , CM000665.1:g.71830631G>T GRCh37
NC_000003.10:g.71913321G>T NCBI36
NG_008275.1:g.8727C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000295619.4:c.209C>A MANE Select ENSP00000295619.3:p.Pro70Gln
ENST00000295619.3:c.209C>A ENSP00000295619.3:p.Pro70Gln
ENST00000353065.7:c.209C>A ENSP00000295618.3:p.Pro70Gln
NM_001126128.1:c.209C>A NP_001119600.1:p.Pro70Gln
NM_021935.3:c.209C>A NP_068754.1:p.Pro70Gln
XM_017006974.1:c.149C>A XP_016862463.1:p.Pro50Gln
NM_001126128.2:c.209C>A MANE Select NP_001119600.1:p.Pro70Gln
NM_021935.4:c.209C>A NP_068754.1:p.Pro70Gln
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