Canonical Allele Identifier: CA2157122296

Gene: VRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.96876100_96876103delinsCAGA , CM000676.2:g.96876100_96876103delinsCAGA	GRCh38
NC_000014.8:g.97342437_97342440delinsCAGA , CM000676.1:g.97342437_97342440delinsCAGA	GRCh37
NC_000014.7:g.96412190_96412193delinsCAGA	NCBI36
NG_016293.1:g.83754_83757delinsCAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216639.8:c.1139_1142delinsCAGA MANE Select	ENSP00000216639.3:p.Thr380=
ENST00000553683.2:c.1139_1142delinsCAGA	ENSP00000451412.2:p.Thr380=
ENST00000555067.2:n.11193_11196delinsCAGA
ENST00000679365.1:c.1130_1133delinsCAGA	ENSP00000505882.1:p.Thr377=
ENST00000679462.1:c.1174_1177delinsCAGA	ENSP00000506011.1:p.Gln392=
ENST00000679506.1:n.3198_3201delinsCAGA
ENST00000679533.1:c.*912_*915delinsCAGA	ENSP00000505873.1:n.*912_*915delinsCAGA
ENST00000679650.1:c.*828_*831delinsCAGA	ENSP00000505156.1:n.*828_*831delinsCAGA
ENST00000679727.1:c.1133_1136delinsCAGA	ENSP00000505844.1:p.Thr378=
ENST00000679758.1:c.1068+15365_1068+15368delinsCAGA	ENSP00000505539.1:n.1068+15365_1068+15368delinsCAGA
ENST00000679770.1:c.1139_1142delinsCAGA	ENSP00000505214.1:p.Thr380=
ENST00000679816.1:c.1139_1142delinsCAGA	ENSP00000506525.1:p.Thr380=
ENST00000679843.1:c.442_445delinsCAGA	ENSP00000506467.1:n.442_445delinsCAGA
ENST00000679903.1:c.1130_1133delinsCAGA	ENSP00000506022.1:p.Thr377=
ENST00000679918.1:c.1139_1142delinsCAGA	ENSP00000505439.1:p.Thr380=
ENST00000679941.1:c.1068+15365_1068+15368delinsCAGA	ENSP00000506520.1:n.1068+15365_1068+15368delinsCAGA
ENST00000679977.1:c.*385_*388delinsCAGA	ENSP00000504897.1:n.*385_*388delinsCAGA
ENST00000680007.1:c.1139_1142delinsCAGA	ENSP00000505683.1:p.Thr380=
ENST00000680335.1:c.1068+15365_1068+15368delinsCAGA	ENSP00000505806.1:n.1068+15365_1068+15368delinsCAGA
ENST00000680387.1:c.1136_1139delinsCAGA	ENSP00000504908.1:p.Thr379=
ENST00000680526.1:c.*587+15436_*587+15439delinsCAGA	ENSP00000505595.1:n.*587+15436_*587+15439delinsCAGA
ENST00000680538.1:c.1049_1052delinsCAGA	ENSP00000505611.1:p.Thr350=
ENST00000680683.1:c.1139_1142delinsCAGA	ENSP00000506334.1:p.Thr380=
ENST00000680724.1:c.1139_1142delinsCAGA	ENSP00000504891.1:p.Thr380=
ENST00000680756.1:c.1139_1142delinsCAGA	ENSP00000506648.1:p.Thr380=
ENST00000680849.1:c.1136_1139delinsCAGA	ENSP00000505602.1:p.Thr379=
ENST00000680851.1:c.1069-5077_1069-5074delinsCAGA	ENSP00000505159.1:n.1069-5077_1069-5074delinsCAGA
ENST00000680922.1:c.*212+15365_*212+15368delinsCAGA	ENSP00000506480.1:n.*212+15365_*212+15368delinsCAGA
ENST00000680993.1:c.*432+15365_*432+15368delinsCAGA	ENSP00000505511.1:n.*432+15365_*432+15368delinsCAGA
ENST00000681061.1:c.692+15365_692+15368delinsCAGA
ENST00000681101.1:c.1139_1142delinsCAGA	ENSP00000506564.1:p.Thr380=
ENST00000681195.1:c.1136_1139delinsCAGA	ENSP00000504933.1:p.Thr379=
ENST00000681249.1:c.1136_1139delinsCAGA	ENSP00000506013.1:p.Thr379=
ENST00000681344.1:c.1139_1142delinsCAGA	ENSP00000506151.1:p.Thr380=
ENST00000681355.1:c.1139_1142delinsCAGA	ENSP00000506214.1:p.Thr380=
ENST00000681363.1:c.*239_*242delinsCAGA	ENSP00000505564.1:n.*239_*242delinsCAGA
ENST00000681419.1:c.1139_1142delinsCAGA	ENSP00000505512.1:p.Thr380=
ENST00000681474.1:c.*51_*54delinsCAGA	ENSP00000505569.1:n.*51_*54delinsCAGA
ENST00000681493.1:c.1133_1136delinsCAGA	ENSP00000506429.1:p.Thr378=
ENST00000681524.1:c.*283_*286delinsCAGA	ENSP00000505783.1:n.*283_*286delinsCAGA
ENST00000681538.1:c.*308_*311delinsCAGA	ENSP00000506662.1:n.*308_*311delinsCAGA
ENST00000681598.1:c.*537+15365_*537+15368delinsCAGA	ENSP00000506128.1:n.*537+15365_*537+15368delinsCAGA
ENST00000681677.1:c.763_766delinsCAGA
ENST00000681695.1:c.*729_*732delinsCAGA	ENSP00000506225.1:n.*729_*732delinsCAGA
ENST00000681778.1:c.1068+15365_1068+15368delinsCAGA	ENSP00000506049.1:n.1068+15365_1068+15368delinsCAGA
ENST00000216639.7:c.1139_1142delinsCAGA	ENSP00000216639.3:p.Thr380=
ENST00000553683.1:c.72_75delinsCAGA
ENST00000555067.1:n.369_372delinsCAGA
ENST00000557222.5:c.637+15365_637+15368delinsCAGA
NM_003384.2:c.1139_1142delinsCAGA	NP_003375.1:p.Thr380=
XM_006720247.2:c.1139_1142delinsCAGA	XP_006720310.1:p.Thr380=
XM_011537132.1:c.1136_1139delinsCAGA	XP_011535434.1:p.Thr379=
XM_006720247.4:c.1139_1142delinsCAGA	XP_006720310.1:p.Thr380=
XM_017021624.2:c.1136_1139delinsCAGA	XP_016877113.1:p.Thr379=
XM_017021625.1:c.1145_1148delinsCAGA	XP_016877114.1:p.Thr382=
XR_001750539.2:n.1086_1089delinsCAGA
NM_003384.3:c.1139_1142delinsCAGA MANE Select	NP_003375.1:p.Thr380=