Canonical Allele Identifier: CA1253627609
Gene: VRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.57980867C= , CM000664.2:g.57980867C= GRCh38
NC_000002.11:g.58208002C= , CM000664.1:g.58208002C= GRCh37
NC_000002.10:g.58061506C= NCBI36
NG_029717.2:g.78127C=

Transcript Alleles

HGVS Amino-acid change
ENST00000648897.1:c.-728-37149C= ENSP00000497378.1:n.-728-37149C=
ENST00000417641.6:c.-438-44798C= ENSP00000402375.2:n.-438-44798C=
ENST00000435505.6:c.-556-44798C= ENSP00000408002.2:n.-556-44798C=
ENST00000463222.1:n.185-44798C=
ENST00000478687.5:n.189-37149C=
NM_001288837.1:c.-556-44798C= NP_001275766.1:n.-556-44798C=
NM_001288838.1:c.-438-44798C= NP_001275767.1:n.-438-44798C=
XR_940118.1:n.241-43733G=
XR_940119.1:n.241-43733G=
XR_940120.1:n.214-43733G=
XR_940121.1:n.355-43733G=
XR_940122.1:n.250-43733G=
NM_001288837.2:c.-556-44798C= NP_001275766.1:n.-556-44798C=
NM_001288838.2:c.-438-44798C= NP_001275767.1:n.-438-44798C=