Canonical Allele Identifier: CA14045156

Gene: VRK1

Linked Data

• dbSNP Id: rs8016620
• gnomAD v2: 14-97393685-C-T
• gnomAD v3: 14-96927348-C-T
• gnomAD v4: 14-96927348-C-T
• MyVariant Identifiers: chr14:g.97393685C>T (hg19) ; chr14:g.96927348C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.96927348C>T , CM000676.2:g.96927348C>T	GRCh38
NC_000014.8:g.97393685C>T , CM000676.1:g.97393685C>T	GRCh37
NC_000014.7:g.96463438C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000679365.1:c.1151-3983C>T	ENSP00000505882.1:n.1151-3983C>T
ENST00000679758.1:c.1069-16169C>T	ENSP00000505539.1:n.1069-16169C>T
ENST00000679843.1:c.463-16169C>T	ENSP00000506467.1:n.463-16169C>T
ENST00000679941.1:c.1069-3983C>T	ENSP00000506520.1:n.1069-3983C>T
ENST00000680335.1:c.1069-3983C>T	ENSP00000505806.1:n.1069-3983C>T
ENST00000680387.1:c.1157-3983C>T	ENSP00000504908.1:n.1157-3983C>T
ENST00000680526.1:c.*588-16169C>T	ENSP00000505595.1:n.*588-16169C>T
ENST00000680922.1:c.*213-16169C>T	ENSP00000506480.1:n.*213-16169C>T
ENST00000680993.1:c.*433-3983C>T	ENSP00000505511.1:n.*433-3983C>T
ENST00000681061.1:c.693-16169C>T
ENST00000681101.1:c.1160-3983C>T	ENSP00000506564.1:n.1160-3983C>T
ENST00000681598.1:c.*538-16169C>T	ENSP00000506128.1:n.*538-16169C>T
ENST00000681677.1:c.784-3983C>T
ENST00000681778.1:c.1069-3983C>T	ENSP00000506049.1:n.1069-3983C>T
ENST00000557222.5:c.638-3983C>T