Canonical Allele Identifier: CA1253627614
Gene: VRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.57980877T= , CM000664.2:g.57980877T= GRCh38
NC_000002.11:g.58208012T= , CM000664.1:g.58208012T= GRCh37
NC_000002.10:g.58061516T= NCBI36
NG_029717.2:g.78137T=

Transcript Alleles

HGVS Amino-acid change
ENST00000648897.1:c.-728-37139T= ENSP00000497378.1:n.-728-37139T=
ENST00000417641.6:c.-438-44788T= ENSP00000402375.2:n.-438-44788T=
ENST00000435505.6:c.-556-44788T= ENSP00000408002.2:n.-556-44788T=
ENST00000463222.1:n.185-44788T=
ENST00000478687.5:n.189-37139T=
NM_001288837.1:c.-556-44788T= NP_001275766.1:n.-556-44788T=
NM_001288838.1:c.-438-44788T= NP_001275767.1:n.-438-44788T=
XR_940118.1:n.241-43743A=
XR_940119.1:n.241-43743A=
XR_940120.1:n.214-43743A=
XR_940121.1:n.355-43743A=
XR_940122.1:n.250-43743A=
NM_001288837.2:c.-556-44788T= NP_001275766.1:n.-556-44788T=
NM_001288838.2:c.-438-44788T= NP_001275767.1:n.-438-44788T=