Canonical Allele Identifier: CA2797413944
Gene: MVK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109586222_109586223del , CM000674.2:g.109586222_109586223del GRCh38
NC_000012.11:g.110024027_110024028del , CM000674.1:g.110024027_110024028del GRCh37
NC_000012.10:g.108508410_108508411del NCBI36
NG_007702.1:g.17528_17529del , LRG_156:g.17528_17529del

Transcript Alleles

HGVS Amino-acid Change
ENST00000539696.6:c.-91-4624_-91-4623del ENSP00000439134.1:n.-91-4624_-91-4623del
ENST00000546277.6:c.631+97_631+98del ENSP00000438153.2:n.631+97_631+98del
ENST00000636529.2:n.182+97_182+98del
ENST00000697195.1:c.*395+97_*395+98del ENSP00000513181.1:n.*395+97_*395+98del
ENST00000697196.1:c.631+97_631+98del ENSP00000513182.1:n.631+97_631+98del
ENST00000228510.8:c.631+97_631+98del MANE Select ENSP00000228510.3:n.631+97_631+98del
ENST00000636529.1:c.168+97_168+98del
ENST00000636996.1:c.479+97_479+98del
ENST00000228510.7:c.631+97_631+98del ENSP00000228510.3:n.631+97_631+98del
ENST00000392727.7:c.475+97_475+98del ENSP00000376487.3:n.475+97_475+98del
ENST00000447878.6:c.*78+97_*78+98del ENSP00000415555.2:n.*78+97_*78+98del
ENST00000537237.5:c.*395+97_*395+98del ENSP00000445382.1:n.*395+97_*395+98del
ENST00000539575.4:c.631+97_631+98del ENSP00000443551.2:n.631+97_631+98del
ENST00000539696.5:c.-91-4624_-91-4623del ENSP00000439134.1:n.-91-4624_-91-4623del
ENST00000545516.1:n.176+97_176+98del
ENST00000545774.5:c.*78+97_*78+98del ENSP00000443978.1:n.*78+97_*78+98del
ENST00000625889.2:c.475+97_475+98del ENSP00000486846.1:n.475+97_475+98del
ENST00000629016.2:c.*78+97_*78+98del ENSP00000486804.1:n.*78+97_*78+98del
NM_000431.3:c.631+97_631+98del NP_000422.1:n.631+97_631+98del
NM_001114185.2:c.631+97_631+98del NP_001107657.1:n.631+97_631+98del
NM_001301182.1:c.475+97_475+98del NP_001288111.1:n.475+97_475+98del
XM_011538372.1:c.631+97_631+98del XP_011536674.1:n.631+97_631+98del
XM_017019313.2:c.475+97_475+98del XP_016874802.1:n.475+97_475+98del
XM_017019314.1:c.631+97_631+98del XP_016874803.1:n.631+97_631+98del
XM_024448982.1:c.631+97_631+98del XP_024304750.1:n.631+97_631+98del
NM_000431.4:c.631+97_631+98del MANE Select NP_000422.1:n.631+97_631+98del
NM_001114185.3:c.631+97_631+98del NP_001107657.1:n.631+97_631+98del
NM_001301182.2:c.475+97_475+98del NP_001288111.1:n.475+97_475+98del