Canonical Allele Identifier: CA434161367
Gene: PROK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.71830627C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.71781476C>T , CM000665.2:g.71781476C>T GRCh38
NC_000003.11:g.71830627C>T , CM000665.1:g.71830627C>T GRCh37
NC_000003.10:g.71913317C>T NCBI36
NG_008275.1:g.8731G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295619.4:c.213G>A MANE Select ENSP00000295619.3:p.Leu71=
ENST00000295619.3:c.213G>A ENSP00000295619.3:p.Leu71=
ENST00000353065.7:c.213G>A ENSP00000295618.3:p.Leu71=
NM_001126128.1:c.213G>A NP_001119600.1:p.Leu71=
NM_021935.3:c.213G>A NP_068754.1:p.Leu71=
XM_017006974.1:c.153G>A XP_016862463.1:p.Leu51=
NM_001126128.2:c.213G>A MANE Select NP_001119600.1:p.Leu71=
NM_021935.4:c.213G>A NP_068754.1:p.Leu71=