Canonical Allele Identifier: CA2797413909
Gene: MVK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109586184_109586185insA , CM000674.2:g.109586184_109586185insA GRCh38
NC_000012.11:g.110023989_110023990insA , CM000674.1:g.110023989_110023990insA GRCh37
NC_000012.10:g.108508372_108508373insA NCBI36
NG_007702.1:g.17490_17491insA , LRG_156:g.17490_17491insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000539696.6:c.-91-4662_-91-4661insA ENSP00000439134.1:n.-91-4662_-91-4661insA
ENST00000546277.6:c.631+59_631+60insA ENSP00000438153.2:n.631+59_631+60insA
ENST00000636529.2:n.182+59_182+60insA
ENST00000697195.1:c.*395+59_*395+60insA ENSP00000513181.1:n.*395+59_*395+60insA
ENST00000697196.1:c.631+59_631+60insA ENSP00000513182.1:n.631+59_631+60insA
ENST00000228510.8:c.631+59_631+60insA MANE Select ENSP00000228510.3:n.631+59_631+60insA
ENST00000636529.1:c.168+59_168+60insA
ENST00000636996.1:c.479+59_479+60insA
ENST00000228510.7:c.631+59_631+60insA ENSP00000228510.3:n.631+59_631+60insA
ENST00000392727.7:c.475+59_475+60insA ENSP00000376487.3:n.475+59_475+60insA
ENST00000447878.6:c.*78+59_*78+60insA ENSP00000415555.2:n.*78+59_*78+60insA
ENST00000537237.5:c.*395+59_*395+60insA ENSP00000445382.1:n.*395+59_*395+60insA
ENST00000539575.4:c.631+59_631+60insA ENSP00000443551.2:n.631+59_631+60insA
ENST00000539696.5:c.-91-4662_-91-4661insA ENSP00000439134.1:n.-91-4662_-91-4661insA
ENST00000545516.1:n.176+59_176+60insA
ENST00000545774.5:c.*78+59_*78+60insA ENSP00000443978.1:n.*78+59_*78+60insA
ENST00000625889.2:c.475+59_475+60insA ENSP00000486846.1:n.475+59_475+60insA
ENST00000629016.2:c.*78+59_*78+60insA ENSP00000486804.1:n.*78+59_*78+60insA
NM_000431.3:c.631+59_631+60insA NP_000422.1:n.631+59_631+60insA
NM_001114185.2:c.631+59_631+60insA NP_001107657.1:n.631+59_631+60insA
NM_001301182.1:c.475+59_475+60insA NP_001288111.1:n.475+59_475+60insA
XM_011538372.1:c.631+59_631+60insA XP_011536674.1:n.631+59_631+60insA
XM_017019313.2:c.475+59_475+60insA XP_016874802.1:n.475+59_475+60insA
XM_017019314.1:c.631+59_631+60insA XP_016874803.1:n.631+59_631+60insA
XM_024448982.1:c.631+59_631+60insA XP_024304750.1:n.631+59_631+60insA
NM_000431.4:c.631+59_631+60insA MANE Select NP_000422.1:n.631+59_631+60insA
NM_001114185.3:c.631+59_631+60insA NP_001107657.1:n.631+59_631+60insA
NM_001301182.2:c.475+59_475+60insA NP_001288111.1:n.475+59_475+60insA