Canonical Allele Identifier: CA353500967

Gene: PROK2

Linked Data

• MyVariant Identifiers: chr3:g.71830629G>T (hg19) ; chr3:g.71781478G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.71781478G>T , CM000665.2:g.71781478G>T	GRCh38
NC_000003.11:g.71830629G>T , CM000665.1:g.71830629G>T	GRCh37
NC_000003.10:g.71913319G>T	NCBI36
NG_008275.1:g.8729C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295619.4:c.211C>A MANE Select	ENSP00000295619.3:p.Leu71Met
ENST00000295619.3:c.211C>A	ENSP00000295619.3:p.Leu71Met
ENST00000353065.7:c.211C>A	ENSP00000295618.3:p.Leu71Met
NM_001126128.1:c.211C>A	NP_001119600.1:p.Leu71Met
NM_021935.3:c.211C>A	NP_068754.1:p.Leu71Met
XM_017006974.1:c.151C>A	XP_016862463.1:p.Leu51Met
NM_001126128.2:c.211C>A MANE Select	NP_001119600.1:p.Leu71Met
NM_021935.4:c.211C>A	NP_068754.1:p.Leu71Met